Organometallic compound, organic light-emitting device including the organometallic compound, diagnostic composition including the organometallic compound

ABSTRACT

An organometallic compound represented by Formula 1, an organic light-emitting device including the organometallic compound, and a diagnostic composition including the organometallic compound:M(L1)n1(L2)n2  Formula 1wherein, in Formula 1, M, L1, L2, n1, and n2 are each described herein.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority and the benefit of Korean Patent Application No. 10-2019-0042745, filed on Apr. 11, 2019, in the Korean Intellectual Property Office, and all the benefits accruing therefrom under 35 U.S.C. § 119, the content of which in its entirety is herein incorporated by reference.

BACKGROUND 1. Field

One or more embodiments relate to an organometallic compound, an organic light-emitting device including the organometallic compound, and a diagnostic composition including the organometallic compound.

2. Description of the Related Art

Organic light-emitting devices are self-emission devices, which have excellent characteristics in terms of a viewing angle, response time, brightness, driving voltage, and response speed, and produce full-color images.

In an example, an organic light-emitting device includes an anode, a cathode, and an organic layer between the anode and the cathode, wherein the organic layer includes an emission layer. A hole transport region may be between the anode and the emission layer, and an electron transport region may be between the emission layer and the cathode. Holes provided from the anode may move toward the emission layer through the hole transport region, and electrons provided from the cathode may move toward the emission layer through the electron transport region. The holes and the electrons recombine in the emission layer to produce excitons. These excitons transit from an excited state to a ground state, thereby generating light.

Luminescent compounds may be used to monitor, sense, or detect a variety of biological materials including cells and proteins. An example of the luminescent compounds is a phosphorescent luminescent compound.

SUMMARY

Aspects of the present disclosure provide a novel organometallic compound, an organic light-emitting device including the novel organometallic compound, and a diagnostic composition including the novel organometallic compound.

Additional aspects will be set forth in part in the description which follows and, in part, will be apparent from the description, or may be learned by practice of the presented embodiments.

An aspect of the present disclosure provides an organometallic compound represented by Formula 1 below: M(L ₁)_(n1)(L ₂)_(n2)  Formula 1

In Formula 1,

M may be a transition metal,

L₁ may be a ligand represented by Formula 2,

n1 may be 1, 2, or 3, wherein, when n1 is 2 or more, two or more L₁(s) may be identical to or different from each other,

L₂ may be a monodentate ligand, a bidentate ligand, a tridentate ligand, or a tetradentate ligand,

n2 may be 0, 1, 2, 3, or 4, wherein, when n2 is 2 or more, two or more L₂(s) may be identical to or different from each other, and

L₁ and L₂ may be different from each other:

In Formula 2,

X₁ may be C, N, Si, or P,

X₂₁ may be C or N,

ring CY₁ and ring CY₂₁ may each independently be a C₅-C₃₀ carbocyclic group or a C₂-C₃₀ heterocyclic group,

X₂ and X₃ may each independently be O, S, Se, or C(R₂), wherein X₂ or X₃ may be O, S, or Se,

X₄ may be N or C(R₄),

X₅ may be N or C(R₅),

R₁, R₂, R₄, R₅, and R₂₁ may each independently be hydrogen, deuterium, —F, —C, —Br, —I, —SF₅, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₂-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₂-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), —P(═O)(Q₈)(Q₉) or —P(Q₈)(Q₉),

a1 and a21 may each independently be an integer from 0 to 20,

ring CY₁ and R₂ may not be linked to each other, and R₁ and R₂ may not be linked to each other,

L₁₁ may be a C₅-C₃₀ carbocyclic group that is unsubstituted or substituted with at least one R_(10a) or a C₂-C₃₀ heterocyclic group that is unsubstituted or substituted with at least one R_(10a),

b11 may be an integer from 0 to 10, wherein, when b11 is 0, a group represented by *-(L₁₁)_(b11)-*′ may be a single bond, and when b11 is 2 or more, two or more L₁₁(s) may be identical to or different from each other,

two of a plurality of neighboring R₂₁(s) may optionally be linked to form a C₅-C₃₀ carbocyclic group that is unsubstituted or substituted with at least one R_(10a) or a C₂-C₃₀ heterocyclic group that is unsubstituted or substituted with at least one R_(10a).

R_(10a) may be the same as defined in connection with R₂₁,

* and *′ each indicate a binding site to M in Formula 1,

a substituent(s) of the substituted C₅-C₃₀ carbocyclic group, the substituted C₂-C₃₀ heterocyclic group, the substituted C₁-C₆₀ alkyl group, the substituted C₂-C₆₀ alkenyl group, the substituted C₂-C₆₀ alkynyl group, the substituted C₁-C₆₀ alkoxy group, the substituted C₃-C₁₀ cycloalkyl group, the substituted C₂-C₁₀ heterocycloalkyl group, the substituted C₃-C₁₀ cycloalkenyl group, the substituted C₂-C₁₀ heterocycloalkenyl group, the substituted C₆-C₆₀ aryl group, the substituted C₆-C₆₀ aryloxy group, the substituted C₆-C₆₀ arylthio group, the substituted C₁-C₆₀ heteroaryl group, the substituted monovalent non-aromatic condensed polycyclic group, and substituted monovalent non-aromatic condensed heteropolycyclic group may be:

-   -   deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H,         —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino         group, an amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, or a C₁-C₆₀ alkoxy group;     -   a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, or a C₁-C₆₀ alkoxy group, each substituted with         deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H,         —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino         group, an amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, a monovalent non-aromatic condensed         heteropolycyclic group, —N(Q₁₁)(Q₁₂), —Si(Q₁₃)(Q₁₄)(Q₁₅),         —B(Q₁₆)(Q₁₇), —P(═O)(Q₁₈)(Q₁₉), or any combination thereof;     -   a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, or a monovalent non-aromatic         condensed heteropolycyclic group;     -   a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, or a monovalent non-aromatic         condensed heteropolycyclic group, each substituted with         deuterium, —F, —C, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H,         —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino         group, an amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a         C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a         C₂-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀         aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl         group, a monovalent non-aromatic condensed polycyclic group, a         monovalent non-aromatic condensed heteropolycyclic group,         —N(Q₂₁)(Q₂₂), —Si(Q₂₃)(Q₂₄)(Q₂₅), —B(Q₂₆)(Q₂₇),         —P(═O)(Q₂₈)(Q₂₉), or any combination thereof;     -   —N(Q₃₁)(Q₃₂), —Si(Q₃₃)(Q₃₄)(Q₃₅), —B(Q₃₆)(Q₃₇), or         —P(═O)(Q₃₈)(Q₃₉); or     -   any combination thereof, and     -   Q₁ to Q₉, Q₁₁ to Q₁₉, Q₂₁ to Q₂₉, and Q₃₁ to Q₃₉ may each         independently be hydrogen, deuterium, —F, —Cl, —Br, —I, a         hydroxyl group, a cyano group, a nitro group, an amino group, an         amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a         C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a         C₂-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀         aryl group substituted with a C₁-C₆₀ alkyl group, a C₆-C₆₀ aryl         group or any combination thereof, a C₆-C₆₀ aryloxy group, a         C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent         non-aromatic condensed polycyclic group, a monovalent         non-aromatic condensed heteropolycyclic group, or any         combination thereof.

Another aspect of the present disclosure provides an organic light-emitting device including: a first electrode; a second electrode; and an organic layer disposed between the first electrode and the second electrode and including an emission layer, wherein the organic layer may include at least one organometallic compound represented by Formula 1.

The organometallic compound included in the emission layer of the organic layer may act as a dopant.

Another aspect of the present disclosure provides a diagnostic composition including at least one organometallic compound represented by Formula 1.

BRIEF DESCRIPTION OF THE DRAWING

These and/or other aspects will become apparent and more readily appreciated from the following description of the embodiments, taken in conjunction with FIGURE which is a schematic cross-sectional view of an organic light-emitting device according to an embodiment.

DETAILED DESCRIPTION

Reference will now be made in detail to embodiments, examples of which are illustrated in the accompanying drawings, wherein like reference numerals refer to like elements throughout. In this regard, the present embodiments may have different forms and should not be construed as being limited to the descriptions set forth herein. Accordingly, the embodiments are merely described below, by referring to the FIGURES, to explain aspects of the present description. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items. Expressions such as “at least one of,” when preceding a list of elements, modify the entire list of elements and do not modify the individual elements of the list.

It will be understood that when an element is referred to as being “on” another element, it can be directly on the other element or intervening elements may be present therebetween. In contrast, when an element is referred to as being “directly on” another element, there are no intervening elements present.

It will be understood that, although the terms “first,” “second,” “third” etc. may be used herein to describe various elements, components, regions, layers and/or sections, these elements, components, regions, layers and/or sections should not be limited by these terms. These terms are only used to distinguish one element, component, region, layer, or section from another element, component, region, layer, or section. Thus, “a first element,” “component,” “region,” “layer,” or “section” discussed below could be termed a second element, component, region, layer, or section without departing from the teachings herein.

The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting. As used herein, the singular forms “a,” “an,” and “the” are intended to include the plural forms, including “at least one,” unless the content clearly indicates otherwise. “At least one” is not to be construed as limiting “a” or “an.” “Or” means “and/or.” As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items. It will be further understood that the terms “comprises” and/or “comprising,” or “includes” and/or “including” when used in this specification, specify the presence of stated features, regions, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, regions, integers, steps, operations, elements, components, and/or groups thereof.

Furthermore, relative terms, such as “lower” or “bottom” and “upper” or “top,” may be used herein to describe one element's relationship to another element as illustrated in the FIGURES. It will be understood that relative terms are intended to encompass different orientations of the device in addition to the orientation depicted in the FIGURES. For example, if the device in one of the FIGURES is turned over, elements described as being on the “lower” side of other elements would then be oriented on “upper” sides of the other elements. The exemplary term “lower,” can therefore, encompasses both an orientation of “lower” and “upper,” depending on the particular orientation of the FIGURE. Similarly, if the device in one of the FIGURES is turned over, elements described as “below” or “beneath” other elements would then be oriented “above” the other elements. The exemplary terms “below” or “beneath” can, therefore, encompass both an orientation of above and below.

“About” or “approximately” as used herein is inclusive of the stated value and means within an acceptable range of deviation for the particular value as determined by one of ordinary skill in the art, considering the measurement in question and the error associated with measurement of the particular quantity (i.e., the limitations of the measurement system). For example, “about” can mean within one or more standard deviations, or within ±30%, 20%, 10%, or 5% of the stated value.

Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and the present disclosure, and will not be interpreted in an idealized or overly formal sense unless expressly so defined herein.

Exemplary embodiments are described herein with reference to cross section illustrations that are schematic illustrations of idealized embodiments. As such, variations from the shapes of the illustrations as a result, for example, of manufacturing techniques and/or tolerances, are to be expected. Thus, embodiments described herein should not be construed as limited to the particular shapes of regions as illustrated herein but are to include deviations in shapes that result, for example, from manufacturing. For example, a region illustrated or described as flat may, typically, have rough and/or nonlinear features. Moreover, sharp angles that are illustrated may be rounded. Thus, the regions illustrated in the FIGURES are schematic in nature and their shapes are not intended to illustrate the precise shape of a region and are not intended to limit the scope of the present claims.

An aspect of the present disclosure provides an organometallic compound represented by Formula 1 below: M(L ₁)_(n1)(L ₂)_(n2)  Formula 1

M in Formula 1 may be a transition metal.

For example, M may be a first-row transition metal, a second-row transition metal, or a third-row transition metal of the Periodic Table of Elements.

In one embodiment, M may be iridium (Ir), platinum (Pt), osmium (Os), titanium (Ti), zirconium (Zr), hafnium (Hf), europium (Eu), terbium (Tb), thulium (Tm), or rhodium (Rh).

In one embodiment, M may be Ir, Pt, Os, or Rh, but embodiments of the present disclosure are not limited thereto.

L₁ in Formula 1 may be a ligand represented by Formula 2, and n1 in Formula 1 indicates the number of L₁ in Formula 1 and may be 1, 2, or 3. When n1 is 2 or more, two or more L₁(s) may be identical to or different from each other:

Formula 2 may be the same as described below.

For example, n1 may be 1 or 2.

L₂ in Formula 1 may be a monodentate ligand, a bidentate ligand, a tridentate ligand, or a tetradentate ligand, and n2 in Formula 1 indicates the number of L₂ and may be 0, 1, 2, 3, or 4. When n2 is 2 or more, two or more L₂(s) may be identical to or different from each other. L₂ may be the same as described below.

For example, n2 in Formula 1 may be 1 or 2.

In Formula 1, L₁ and L₂ may be different from each other.

In one embodiment, M may be Ir or Os, and the sum of n1 and n2 may be 3 or 4; or M may be Pt, and the sum of n1 and n2 may be 2.

In Formula 2, X₁ may be C, N, Si, or P, and X₂₁ may be C or N.

For example, in Formula 2, X₂₁ may be C.

In Formula 2, ring CY₁ and ring CY₂₁ may each independently be a C₅-C₃₀ carbocyclic group or a C₂-C₃₀ heterocyclic group.

For example, ring CY₁ and ring CY₂₁ may each independently be i) a first ring, ii) a second ring, iii) a condensed ring in which at least two first rings are condensed with each other, iv) a condensed ring in which at least two second rings are condensed with each other, or v) a condensed ring in which at least one first ring and at least one second ring are condensed with each other.

The first ring may be a cyclopentane group, a cyclopentadiene group, a furan group, a thiophene group, a pyrrole group, a silole group, an indene group, a benzofuran group, a benzothiophene group, an indole group, a benzosilole group, an oxazole group, an isoxazole group, an oxadiazole group, an isoxadiazole group, an oxatriazole group, an isoxatriazole group, a thiazole group, an isothiazole group, a thiadiazole group, an isothiadiazole group, a thiatriazole group, an isothiatriazole group, a pyrazole group, an imidazole group, a triazole group, a tetrazole group, an azasilole group, a diazasilole group, or a triazasilole group.

The second ring may be an adamantane group, a norbornane group, a norbornene group, a cyclohexane group, a cyclohexene group, a benzene group, a pyridine group, a pyrimidine group, a pyrazine group, a pyridazine group, or a triazine group.

In one embodiment, ring CY₁ and ring CY₂₁ may each independently be a cyclopentene group, a cyclohexene group, a benzene group, a naphthalene group, an anthracene group, a phenanthrene group, a triphenylene group, a pyrene group, a chrysene group, a cyclopentadiene group, a 1,2,3,4-tetrahydronaphthalene group, a thiophene group, a furan group, an indole group, a benzoborole group, a benzophosphole group, an indene group, a benzosilole group, a benzogermole group, a benzothiophene group, a benzoselenophene group, a benzofuran group, a carbazole group, a dibenzoborole group, a dibenzophosphole group, a fluorene group, a dibenzosilole group, a dibenzogermole group, a dibenzothiophene group, a dibenzoselenophene group, a dibenzofuran group, a dibenzothiophene 5-oxide group, a 9H-fluorene-9-one group, a dibenzothiophene 5,5-dioxide group, an azaindole group, an azabenzoborole group, an azabenzophosphole group, an azaindene group, an azabenzosilole group, an azabenzogermole group, an azabenzothiophene group, an azabenzoselenophene group, an azabenzofuran group, an azacarbazole group, an azadibenzoborole group, an azadibenzophosphole group, an azafluorene group, an azadibenzosilole group, an azadibenzogermole group, an azadibenzothiophene group, an azadibenzoselenophene group, an azadibenzofuran group, an azadibenzothiophene 5-oxide group, an aza-9H-fluorene-9-one group, an azadibenzothiophene 5,5-dioxide group, a pyridine group, a pyrimidine group, a pyrazine group, a pyridazine group, a triazine group, a quinoline group, an isoquinoline group, a quinoxaline group, a quinazoline group, a phenanthroline group, a pyrrole group, a pyrazole group, an imidazole group, a triazole group, an oxazole group, an isoxazole group, a thiazole group, an isothiazole group, an oxadiazole group, a thiadiazole group, a benzopyrazole group, a benzimidazole group, a benzoxazole group, a benzothiazole group, a benzoxadiazole group, a benzothiadiazole group, a 5,6,7,8-tetrahydroisoquinoline group, or a 5,6,7,8-tetrahydroquinoline group, but embodiments of the present disclosure are not limited thereto.

In one or more embodiments, ring CY₁ may be a cyclopentane group, a cyclohexane group, a cycloheptane group, a cyclooctane group, an adamantane group, a norbornane group, a norbornene group, a cyclopentene group, a cyclohexene group, a cycloheptene group, a benzene group, a naphthalene group, a fluorene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a pyrrole group, a thiophene group, a furan group, an imidazole group, a pyrazole group, a thiazole group, an isothiazole group, an oxazole group, an isoxazole group, a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, an isoindole group, an indole group, an indazole group, a purine group, a quinoline group, an isoquinoline group, a benzoquinoline group, a quinoxaline group, a quinazoline group, a cinnoline group, a carbazole group, a phenanthroline group, a benzimidazole group, a benzofuran group, a benzothiophene group, an isobenzothiazole group, a benzoxazole group, an isobenzoxazole group, a triazole group a tetrazole group, an oxadiazole group, a triazine group, a dibenzofuran group, a dibenzothiophene group, a dibenzosilole group, a benzocarbazole group, a dibenzocarbazole group, an imidazopyridine group, or an imidazopyrimidine group, but embodiments of the present disclosure are not limited thereto.

In Formula 2, X₂ and X₃ may each independently be O, S, Se, or C(R₂), wherein X₂ or X₃ may be O, S, or Se.

For example, in Formula 2, i) X₂ may be O, S, or Se, and X₃ may be C(R₂), or ii) X₂ may be C(R₂), and X₃ may be O, S, or Se.

In Formula 2, X₄ may be N or C(R₄), and X₅ may be N or C(R₅).

For example, X₄ may be C(R₄), and X₅ may be C(R₅).

In Formula 2, R₁, R₂, R₄, R₅, and R₂₁ may each independently be hydrogen, deuterium, —F, —C, —Br, —I, —SF₅, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₂-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₂-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), —P(═O)(Q₈)(Q₉) or —P(Q₈)(Q₉), wherein Q₁ to Q₉ are each the same as described above.

For example, R₁, R₂, R₄, R₅, R₂₁, and R_(10a) may each independently be:

-   -   hydrogen, deuterium, —F, —C, —Br, —I, a hydroxyl group, a cyano         group, a nitro group, an amino group, an amidino group, a         hydrazine group, a hydrazone group, a carboxylic acid group or a         salt thereof, a sulfonic acid group or a salt thereof, a         phosphoric acid group or a salt thereof, —SF₅, a C₁-C₂₀ alkyl         group, or a C₁-C₂₀ alkoxy group;     -   a C₁-C₂₀ alkyl group or a C₁-C₂₀ alkoxy group, each substituted         with deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃,         —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an         amino group, an amidino group, a hydrazine group, a hydrazone         group, a carboxylic acid group or a salt thereof, a sulfonic         acid group or a salt thereof, a phosphoric acid group or a salt         thereof, a C₁-C₁₀ alkyl group, a cyclopentyl group, a cyclohexyl         group, a cycloheptyl group, a cycloctyl group, an adamantyl         group, a norbornenyl group, a cyclopentenyl group, a         cyclohexenyl group, a cycloheptenyl group, a         bicyclo[1.1.1]pentyl group, a bicyclo[2.1.1]hexyl group, a         bicyclo[2.2.1]heptyl group, a bicyclo[2.2.2]octyl group, a         phenyl group, a biphenyl group, a terphenyl group, a naphthyl         group, a pyridinyl group, a pyrimidinyl group, or any         combination thereof;     -   a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a         cycloctyl group, an adamantyl group, a norbornenyl group, a         cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl         group, a cyclooctenyl group, a bicyclo[1.1.1]pentyl group, a         bicyclo[2.1.1]hexyl group, a bicyclo[2.2.1]heptyl group, a         bicyclo[2.2.2]octyl group, a phenyl group, a biphenyl group, a         terphenyl group, a naphthyl group, a fluorenyl group, a         phenanthrenyl group, an anthracenyl group, a fluoranthenyl         group, a triphenylenyl group, a pyrenyl group, a chrysenyl         group, a pyrrolyl group, a thiophenyl group, a furanyl group, an         imidazolyl group, a pyrazolyl group, a thiazolyl group, an         isothiazolyl group, an oxazolyl group, an isoxazolyl group, a         pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a         pyridazinyl group, an isoindolyl group, an indolyl group, an         indazolyl group, a purinyl group, a quinolinyl group, an         isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl         group, a quinazolinyl group, a cinnolinyl group, a carbazolyl         group, a phenanthrolinyl group, a benzimidazolyl group, a         benzofuranyl group, a benzothiophenyl group, an         isobenzothiazolyl group, a benzoxazolyl group, an         isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an         oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a         dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, an imidazopyridinyl group, or an         imidazopyrimidinyl group, each unsubstituted or substituted with         deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H,         —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino         group, an amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a cyclopentyl group,         a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an         adamantyl group, a norbornenyl group, a cyclopentenyl group, a         cyclohexenyl group, a cycloheptenyl group, a cyclooctenyl group,         a bicyclo[1.1.1]pentyl group, a bicyclo[2.1.1]hexyl group, a         bicyclo[2.2.1]heptyl group, a bicyclo[2.2.2]octyl group, a         phenyl group, a biphenyl group, a terphenyl group, a naphthyl         group, a fluorenyl group, a phenanthrenyl group, an anthracenyl         group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl         group, a chrysenyl group, a pyrrolyl group, a thiophenyl group,         a furanyl group, an imidazolyl group, a pyrazolyl group, a         thiazolyl group, an isothiazolyl group, an oxazolyl group, an         isoxazolyl group, a pyridinyl group, a pyrazinyl group, a         pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an         indolyl group, an indazolyl group, a purinyl group, a quinolinyl         group, an isoquinolinyl group, a benzoquinolinyl group, a         quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a         carbazolyl group, a phenanthrolinyl group, a benzimidazolyl         group, a benzofuranyl group, a benzothiophenyl group, an         isobenzothiazolyl group, a benzoxazolyl group, an         isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an         oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a         dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, an imidazopyridinyl group, an         imidazopyrimidinyl group, —Si(Q₃₃)(Q₃₄)(Q₃₅), or any combination         thereof; or     -   —N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), —P(═O)(Q₈)(Q₉), or         —P(Q₈)(Q₉), and     -   Q₁ to Q and Q₃₃ to Q₃₅ may each independently be:     -   —CH₃, —CD₃, —CD₂H, —CDH₂, —CH₂CH₃, —CH₂CD₃, —CH₂CD₂H, —CH₂CDH₂,         —CHDCH₃, —CHDCD₂H, —CHDCDH₂, —CHDCD₃, —CD₂CD₃, —CD₂CD₂H, or         —CD₂CDH₂; or     -   an n-propyl group, an isopropyl group, an n-butyl group, an         isobutyl group, a sec-butyl group, a tert-butyl group, an         n-pentyl group, an isopentyl group, a sec-pentyl group, a         tert-pentyl group, a phenyl group, or a naphthyl group, each         unsubstituted or substituted with deuterium, a C₁-C₁₀ alkyl         group, a phenyl group, or any combination thereof, but         embodiments of the present disclosure are not limited thereto.

In Formula 2, a1 and a21 each indicate the number of R₁ and the number of R₂₁, respectively, and may each independently be an integer from 0 to 20 (for example, an integer from 0 to 10 or an integer from 0 to 5). When a1 is 2 or more, two or more R₁(s) may be identical to or different from each other, and when a21 is 2 or more, two or more R₂₁(s) may be identical to or different from each other.

In Formula 2, ring CY₁ and R₂ are not linked to each other, and R₁ and R₂ are not linked to each other.

In one embodiment, a group represented by

in Formula 2 may be a C₂-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a C₆-C₃₀ aryl group, a C₂-C₃₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, or a monovalent non-aromatic condensed heteropolycyclic group, each unsubstituted or substituted with R₁(s) in the number of a1.

In Formula 2, R₁ and R₂ may each independently be:

-   -   hydrogen, deuterium, —F, —C, —Br, —I, a cyano group, or —SF₅, or     -   a C₁-C₆₀ alkyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl         group, a C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl         group, or a C₂-C₁₀ heterocycloalkenyl group, each unsubstituted         or substituted with deuterium, —F, —C, —Br, —I, —CD₃, —CD₂H,         —CDH₂, —CF₃, —CF₂H, —CFH₂, a cyano group, a C₁-C₂₀ alkyl group,         a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a         cycloctyl group, an adamantyl group, a norbornyl group, a         norbornenyl group, a cyclopentenyl group, a cyclohexenyl group,         a cycloheptenyl group, a phenyl group, a biphenyl group, a         naphthyl group, a pyridinyl group, a pyrimidinyl group, or any         combination thereof, and     -   a1 may be an integer from 0 to 10.

Detailed descriptions of a1, R₁, a C₁-C₆₀ alkyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a C₂-C₁₀ heterocycloalkenyl group, a C₃-C₁₀ cycloalkenyl group, a C₆-C₃₀ aryl group, a C₂-C₃₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group are the same as described above.

In one or more embodiments, a group represented by

in Formula 2 may be a phenyl group, a biphenyl group, a naphthyl group, a fluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthrolinyl group, a benzimidazolyl group, a benzofuranyl group, a benzothiophenyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, an imidazopyridinyl group, or an imidazopyrimidinyl group, each unsubstituted or substituted with R₁(s) in the number of a1.

In Formula 2, R₁ and R₂ may each independently be:

-   -   hydrogen, deuterium, —F, —C, —Br, —I, a cyano group, or —SF₅, or     -   a methyl group, an ethyl group, a propyl group, an n-butyl         group, an isobutyl group, a sec-butyl group, a tert-butyl group,         an n-pentyl group, an isopentyl group, a sec-pentyl group, a         tert-pentyl group, an n-hexyl group, an isohexyl group, a         sec-hexyl group, a tert-hexyl group, an n-heptyl group, an         isoheptyl group, a sec-heptyl group, a tert-heptyl group, an         n-octyl group, an isooctyl group, a sec-octyl group, a         tert-octyl group, an n-nonanyl group (an n-nonyl group), an         isononanyl group (an isononyl group), a sec-nonanyl group (a         sec-nonyl group), a tert-nonanyl group (a tert-nonyl group), an         n-decanyl group, an isodecanyl group, a sec-decanyl group, a         tert-decanyl group, a C₁-C₁₀ alkoxy, a cyclopentyl group, a         cyclohexyl group, a cycloheptyl group, a cycloctyl group, an         adamantyl group, a norbornanyl group, a norbornenyl group, a         cyclopentenyl group, a cyclohexenyl group or a cycloheptenyl         group, each unsubstituted or substituted with deuterium, —F,         —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a cyano         group, a C₁-C₂₀ alkyl group, a cyclopentyl group, a cyclohexyl         group, a cycloheptyl group, a cycloctyl group, an adamantyl         group, a norbornyl group, a norbornenyl group, a cyclopentenyl         group, a cyclohexenyl group, a cycloheptenyl group, a phenyl         group, a biphenyl group, a naphthyl group, a pyridinyl group, a         pyrimidinyl group, or any combination thereof, and     -   a1 may be an integer from 0 to 5, but embodiments of the present         disclosure are not limited thereto.

In one or more embodiments, a group represented by

in Formula 2 may be a group represented by one of Formulae 10-13(1) to 10-13(18) and 10-13:

In Formulae 10-13(1) to 10-13(18) and 10-13, R_(1a) to R_(1e) are each independently the same as defined in connection with R₁, wherein R_(1a) to R_(1e) are not each hydrogen, and * indicates a binding site to a neighboring atom (e.g., carbon atom).

For example, a group represented by

in Formula 2 may be a group represented by one of Formulae 10-13 to 10-240, wherein R₁, R₂, R₄, R₅, R₂₁, and R_(10a) may each independently be hydrogen, deuterium, —F, a cyano group, a nitro group, —SF₅, —CH₃, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a group represented by one of Formulae 9-1 to 9-19, a group represented by one of Formulae 10-1 to 10-240, or —Si(Q₃)(Q₄)(Q₅) (wherein Q₃ to Q₅ are the same as described above), but embodiments of the present disclosure are not limited thereto:

In Formulae 9-1 to 9-19 and 10-1 to 10-240,* indicates a binding site to a neighboring atom, Ph indicates a phenyl group, and TMS indicates a trimethylsilyl group.

In Formula 2, L₁₁ may be a C₅-C₃₀ carbocyclic group that is unsubstituted or substituted with at least one R_(10a) or a C₂-C₃₀ heterocyclic group that is unsubstituted or substituted with at least one R_(10a), wherein R_(10a) is the same as described above.

For example, L₁₁ may be a benzene group, a naphthalene group, an anthracene group, a phenanthrene group, a triphenylene group, a pyrene group, a chrysene group, a cyclopentadiene group, a thiophene group, a furan group, an indole group, a benzoborole group, a benzophosphole group, an indene group, a benzosilole group, a benzogermole group, a benzothiophene group, a benzoselenophene group, a benzofuran group, a carbazole group, a dibenzoborole group, a dibenzophosphole group, a fluorene group, a dibenzosilole group, a dibenzogermole group, a dibenzothiophene group, a dibenzoselenophene group, a dibenzofuran group, a dibenzothiophene 5-oxide group, a 9H-fluorene-9-one group, a dibenzothiophene 5,5-dioxide group, an azaindole group, an azabenzoborole group, an azabenzophosphole group, an azaindene group, an azabenzosilole group, an azabenzogermole group, an azabenzothiophene group, an azabenzoselenophene group, an azabenzofuran group, an azacarbazole group, an azadibenzoborole group, an azadibenzophosphole group, an azafluorene group, an azadibenzosilole group, an azadibenzogermole group, an azadibenzothiophene group, an azadibenzoselenophene group, an azadibenzofuran group, an azadibenzothiophene 5-oxide group, an aza-9H-fluorene-9-one group, an azadibenzothiophene 5,5-dioxide group, a pyridine group, a pyrimidine group, a pyrazine group, a pyridazine group, a triazine group, a quinoline group, an isoquinoline group, a quinoxaline group, a quinazoline group, a phenanthroline group, a pyrrole group, a pyrazole group, an imidazole group, a triazole group, an oxazole group, an isoxazole group, a thiazole group, an isothiazole group, an oxadiazole group, a thiadiazole group, a benzopyrazole group, a benzimidazole group, a benzoxazole group, a benzothiazole group, a benzoxadiazole group, or a benzothiadiazole group, each unsubstituted or substituted with at least one R_(10a), but embodiments of the present disclosure are not limited thereto.

In Formula 2, b11 indicates the number of L₁₁, and may be an integer from 0 to 10, wherein, when b11 is 0, a group represented by *-(L₁₁)_(b11)-*′ may be a single bond, and when b11 is 2 or more, two or more L₁₁(s) may be identical to or different from each other. For example, b11 may be 0, 1, 2, or 3, but embodiments of the present disclosure are not limited thereto.

In Formula 2, two of a plurality of neighboring R₂₁(s) may optionally be linked to form a C₅-C₃₀ carbocyclic group that is unsubstituted or substituted with at least one R_(10a) or a C₂-C₃₀ heterocyclic group that is unsubstituted or substituted with at least one R_(10a) (for example, a benzene group, a cyclopentane group, a cyclopentadiene group, a furan group, a thiophene group, a pyrrole group, a silole group, an indene group, a benzofuran group, a benzothiophene group, an indole group, or a benzosilole group, each unsubstituted or substituted with at least one R_(10a), wherein R_(10a) is the same as defined in connection with R₂₁). Detailed descriptions of a C₅-C₃₀ carbocyclic group and a C₂-C₃₀ heterocyclic group are the same as described above.

In Formula 2, * and *′ each indicate a binding site to M in Formula 1.

In one embodiment, a group represented by

in Formula 2 may be a group represented by one of Formulae CY21-1 to CY21-25:

In Formulae CY21-1 to CY21-25,

X₂₁ and R₂₁ may each independently be the same as described herein,

X₂₂ may be C(R₂₂)(R₂₃), N(R₂₂), O, S, or Si(R₂₂)(R₂₃),

R₂₂ to R₂₉ may each independently be the same as defined in connection with R₂₁,

a26 may be an integer from 0 to 6,

a24 may be an integer from 0 to 4,

a23 may be an integer from 0 to 3,

a22 may be an integer from 0 to 2,

*″ indicates a binding site to a carbon atom of a neighboring 6-membered ring in Formula 2, and

* indicates a binding site to M in Formula 1.

In one embodiment, a group represented by

in Formula 2 may be a group represented by one of Formulae CY21(1) to CY21(56) or a group represented by Formulae CY21-20 to CY21-25:

In Formulae CY21(1) to CY21(56),

X₂₁ and R₂₁ may each independently be the same as described herein,

R_(21a) to R_(21d) may each independently be the same as defined in connection with R₂₁, and R₂₁ and R_(21a) to R_(21d) are not each hydrogen,

*″ indicates a binding site to a carbon atom of a neighboring 6-membered ring in Formula 2, and

* indicates a binding site to M in Formula 1.

In one embodiment, a group represented by

in Formula 2 may be a group represented by one of Formulae CY21(1), CY21(3), CY21(10) and a group represented by one of Formulae CY21-20 to CY21-25, but embodiments of the present disclosure are not limited thereto. For example, in Formula CY21(10), R_(21a) and R_(21b) may be identical to or different from each other. In one embodiment, in Formula CY21(10), R_(21a) and R_(21b) may be different from each other, and the number of carbon atoms included in R_(21a) may be larger than the number of carbon atoms included in R_(21b).

In one embodiment, in Formula 1, L₁ may be a ligand represented by Formula 2A or 2B, but embodiments of the present disclosure are not limited thereto:

In Formulae 2A and 2B, X₁, X₂₁, ring CY₁, ring CY₂₁, X₄, X₅, R₁, R₂, R₂₁, a1, a21, L₁₁, b11*, and *′ may each independently be the same as described herein, wherein X₂ and X₃ may each independently be O, S, or Se.

In Formula 1, L₂ may be a bidentate ligand linked to M of Formula 1 via O, S, N, C, P, Si, or As.

In one embodiment, in Formula 1, L₂ may be a bidentate ligand represented by Formula 3:

In Formula 3,

X₃₁ and X₃₂ may each independently be O, S, N, C, P, Si, or As,

indicates an arbitrary atom group linking X₃₁ and X₃₂ to each other, and

* and *′ each indicate a binding site to M in Formula 1.

For example, in Formula 3, i) X₃₁ and X₃₂ may each be O ii) X₃₁ may be O, and X₃₂ may be N, or iii) X₃₁ may be N, and X₃₂ may be C, but embodiments of the present disclosure are not limited thereto.

In one or more embodiments, in Formula 1, L₂ may be a monodentate ligand, for example, I⁻, Br⁻, Cl⁻, sulfide, nitrate, azide, hydroxide, cyanate, isocyanate, thiocyanate, water, acetonitrile, pyridine, ammonia, carbon monoxide, P(Ph)₃, P(Ph)₂CH₃, PPh(CH₃)₂, or P(CH₃)₃, but embodiments of the present disclosure are not limited thereto.

In one or more embodiments, in Formula 1, L₂ may be a bidentate ligand, for example, oxalate, acetylacetonate, picolinic acid, 1,2-bis(diphenylphosphino)ethane, 1,1-bis(diphenylphosphino)methane, glycinate, or ethylenediamine, but embodiments of the present disclosure are not limited thereto.

In one or more embodiments, in Formula 1, L₂ may be a group represented by one of Formulae 3A to 3F:

In Formulae 3A to 3F,

Y₁₃ may be O, N, N(Z₁), P(Z₁)(Z₂), or As(Z₁)(Z₂),

Y₁₄ may be O, N, N(Z₃), P(Z₃)(Z₄), or As(Z₃)(Z₄),

T₁₁ may be a single bond, a double bond, *—C(Z₁₁)(Z₁₂)—*′, *—C(Z₁₁)═C(Z₁₂)—*′, *═C(Z₁₁)—*′, *—C(Z₁₁)═*′, *═C(Z₁₁)—C(Z₁₂)═C(Z₁₃)—*′, *—C(Z₁₁)═C(Z₁₂)—C(Z₁₃)=*′, *—N(Z₁₁)—*′, or a C₅-C₃₀ carbocyclic group that is unsubstituted or substituted with at least one Z₁₁,

a11 may be an integer from 1 to 10,

Y₁₁ and Y₁₂ may each independently be C or N,

T₂₁ may be a single bond, a double bond, O, S, C(Z₁₁)(Z₁₂), Si(Z₁₁)(Z₁₂), or N(Z₁₁),

ring CY₁₁ and ring CY₁₂ may each independently be a C₅-C₃₀ carbocyclic group or a C₂-C₃₀ heterocyclic group,

A₁ may be P or As,

Z₁ to Z₄ and Z₁₁ to Z₁₃ may each independently be the same as defined in connection with R₂₁,

d1 and d2 may each independently be an integer from 0 to 10, and

* and *′ each indicate a binding site to M in Formula 1.

In Formulae 3A to 3F, the C₅-C₃₀ carbocyclic group and the C₂-C₃₀ heterocyclic group may each independently be the same as defined in connection with ring CY₂₁.

For example, a moiety represented by

in Formula 3D may be a group represented by one of Formulae CY11-1 to CY11-34, and/or

a moiety represented by

in Formulae 3C and 3D may be a group represented by Formulae one of CY12-1 to CY12-34:

In Formulae CY11-1 to CY11-34 and CY12-1 to CY12-34,

X₃₁ may be O, S, N(Z₁₁), C(Z₁₁)(Z₁₂), or Si(Z₁₁)(Z₁₂),

X₄₁ may be O, S, N(Z₂₁), C(Z₂₁)(Z₂₂), or Si(Z₂₁)(Z₂₂),

Y₁₁, Y₁₂, Z₁, and Z₂ may each independently be the same as described herein,

Z₁₁ to Z₁₈ and Z₂₁ to Z₂₈ may each independently be the same as defined in connection with R₂₁,

d12 and d22 may each independently be an integer from 0 to 2,

d13 and d23 may each independently be an integer from 0 to 3,

d14 and d24 may each independently be an integer from 0 to 4,

d15 and d25 may each independently be an integer from 0 to 5,

d16 and d26 may each independently be an integer from 0 to 6, and

in Formulae CY11-1 to CY11-34 and CY12-1 to CY12-34, * and *′ each indicate a binding site to M in Formula 1, and *″ indicates a binding site to a neighboring atom in Formula 3C or T₂₁ in Formula 3D.

In one embodiment, in Formula 1, L₂ may be a group represented by one of Formulae 3-1(1) to 3-1(66) and 3-1(301) to 3-1(309), but embodiments of the present disclosure are not limited thereto:

In Formulae 3-1(1) to 3-1(66) and 3-1(301) to 3-1(309),

X₄₁ may be O, S, N(Z₂₁), C(Z₂₁)(Z₂₂), or Si(Z₂₁)(Z₂₂),

Z₁ to Z₄, Z_(1a), Z_(1b), Z_(1c), Z_(1d), Z_(2a), Z_(2b), Z_(2c), Z_(2d), Z₁₁ to Z₁₄, Z₂₁ and Z₂₂ may each independently be the same as defined in connection with R₂₁,

d14 may be an integer from 0 to 4,

d26 may be an integer from 0 to 6, and

* and *′ each indicate a binding site to M in Formula 1.

For example, Z₁₁ and Z₁₃ in Formula 3-1(301) may each independently be a methyl group.

In one embodiment, Z₁₁, Z₁₃, or a combination thereof in Formula 3-1(301) may each independently be a substituted or unsubstituted C₂-C₃₀ alkyl group or a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, but embodiments of the present disclosure are not limited thereto.

In one embodiment, the organometallic compound represented by Formula 1 may emit red light or green light.

The terms “an azaindole group, an azabenzoborole group, an azabenzophosphole group, an azaindene group, an azabenzosilole group, an azabenzogermole group, an azabenzothiophene group, an azabenzoselenophene group, an azabenzofuran group, an azacarbazole group, an azadibenzoborole group, an azadibenzophosphole group, an azafluorene group, an azadibenzosilole group, an azadibenzogermole group, an azadibenzothiophene group, an azadibenzoselenophene group, an azadibenzofuran group, an azadibenzothiophene 5-oxide group, an aza-9H-fluorene-9-one group, and an azadibenzothiophene 5,5-dioxide group” as used herein each refer to a heterocyclic group having the same backbone as “an indole group, a benzoborole group, a benzophosphole group, an indene group, a benzosilole group, a benzogermole group, a benzothiophene group, a benzoselenophene group, a benzofuran group, a carbazole group, a dibenzoborole group, a dibenzophosphole group, a fluorene group, a dibenzosilole group, a dibenzogermole group, a dibenzothiophene group, a dibenzoselenophene group, a dibenzofuran group, a dibenzothiophene 5-oxide group, a 9H-fluorene-9-one group, and a dibenzothiophene 5,5-dioxide group” in which at least one carbon atom constituting the cyclic groups is replaced with N.

In one or more embodiments, the organometallic compound represented by Formula 1 may be one of Compounds 1 to 469, but embodiments of the present disclosure are not limited thereto:

L₁ of the organometallic compound represented by Formula 1 may be a ligand represented by Formula 2A, and n1 which indicates the number of L₁ may be 1, 2, or 3. That is, the organometallic compound includes, as ligands linked to metal M, at least one ligand represented by Formula 2.

X₂ and X₃ in Formula 2 may each independently be O, S, Se, or C(R₂), wherein X₂ or X₃ may be O, S, or Se. That is, in Formula 2, the 5-membered ring (see Formula 2′) does not include *═N—*′ (* and *′ each indicate a binding site to a neighboring atom) as a ring-forming atom, and includes O, S, or Se. In addition, in Formula 2, the 5-membered ring is condensed with the 6-membered ring while sharing carbon 1 and carbon 2 (see Formula 2′). Therefore, a reduction in the intermolecular bonding force of the organometallic compound represented by Formula 1 may be prevented. Therefore, a reduction in the lifespan of an electronic device, for example, an organic light-emitting device, which includes the organometallic compound represented by Formula 1, may be prevented.

The ligand represented by Formula 2 includes “ring CY₁”. Therefore, a transition dipole moment increases in an alignment axis direction of Formula 1, and the alignment of the organometallic compound represented by Formula 1 may be improved, thereby increasing the luminescence efficiency of an electronic device, for example, an organic light-emitting device, which includes the organometallic compound represented by Formula 1.

Meanwhile, in Formula 2, ring CY₁ and R₂ are not linked to each other, and R₁ and R₂ are not linked to each other. Therefore, it is possible to prevent the transition dipole moment of Formula 1 from being deviated to a direction other than the alignment axis direction of Formula 1, thereby increasing the luminescence efficiency of an electronic device, for example, an organic light-emitting device, which includes at least one organometallic compound represented by Formula 1.

A highest occupied molecular orbital (HOMO) energy level, a lowest unoccupied molecular orbital (LUMO) energy level, and a triplet (T₁) energy level of some compounds of the organometallic compound represented by Formula 1 are evaluated by a density functional theory (DFT) of Gaussian program with molecular structure optimization based on B3LYP, and results are shown in Table 1.

TABLE 1 Compound No. HOMO (eV) LUMO (eV) T₁ (eV) 1 −4.623 −1.748 2.253 16 −4.469 −1.747 2.121 31 −4.614 −1.809 2.215 236 −4.517 −1.786 2.103 346 −4.567 −1.598 2.208 439 −4.618 −1.678 2.235 466 −4.625 −1.770 2.203 467 −4.480 −1.677 2.187 468 −4.811 −1.660 2.278 469 −4.836 −1.637 2.287

Referring to Table 1, it is confirmed that the organometallic compound represented by Formula 1 has such electrical characteristics that are suitable for use in an electronic device, for example, an organic light-emitting device, for use as a dopant.

Synthesis methods of the organometallic compound represented by Formula 1 may be understood by one of ordinary skill in the art by referring to Synthesis Examples provided below.

Therefore, the organometallic compound represented by Formula 1 may be suitable for use in an organic layer of an organic light-emitting device, for example, for use as a dopant in an emission layer of the organic layer. Another aspect of the present disclosure provides an organic light-emitting device including: a first electrode, a second electrode, and an organic layer disposed between the first electrode and the second electrode and including an emission layer, wherein the organic layer includes the organometallic compound represented by Formula 1.

The organic light-emitting device may have, due to the inclusion of an organic layer including the organometallic compound represented by Formula 1, a low driving voltage, high external quantum luminescence efficiency, a low roll-off ratio, and a long lifespan.

The organometallic compound represented by Formula 1 may be used between a pair of electrodes of an organic light-emitting device. For example, the organometallic compound represented by Formula 1 may be included in the emission layer. In this regard, the organometallic compound may act as a dopant, and the emission layer may further include a host (that is, an amount of the organometallic compound represented by Formula 1 is smaller than an amount of the host). The emission layer may emit, for example, green light or red light.

The expression “(an organic layer) includes at least one organometallic compound” as used herein may include a case in which “(an organic layer) includes identical organometallic compounds represented by Formula 1” and a case in which “(an organic layer) includes two or more different organometallic compounds represented by Formula 1”.

For example, the organic layer may include, as the organometallic compound, only Compound 1. In this regard, Compound 1 may exist only in the emission layer of the organic light-emitting device. In one or more embodiments, the organic layer may include, as the organometallic compound, Compound 1 and Compound 2. In this regard, Compound 1 and Compound 2 may exist in an identical layer (for example, Compound 1 and Compound 2 both may exist in an emission layer).

The first electrode may be an anode, which is a hole injection electrode, and the second electrode may be a cathode, which is an electron injection electrode; or the first electrode may be a cathode, which is an electron injection electrode, and the second electrode may be an anode, which is a hole injection electrode.

For example, in the organic light-emitting device, the first electrode is an anode, and the second electrode is a cathode, and the organic layer further includes a hole transport region between the first electrode and the emission layer and an electron transport region between the emission layer and the second electrode, and the hole transport region includes a hole injection layer, a hole transport layer, an electron blocking layer, or any combination thereof, and the electron transport region includes a hole blocking layer, an electron transport layer, an electron injection layer, or any combination thereof.

The term “organic layer” as used herein refers to a single layer and/or a plurality of layers disposed between the first electrode and the second electrode of an organic light-emitting device. The “organic layer” may include, in addition to an organic compound, an organometallic complex including metal.

FIGURE is a schematic cross-sectional view of an organic light-emitting device 10 according to an embodiment. Hereinafter, the structure of an organic light-emitting device according to an embodiment and a method of manufacturing an organic light-emitting device according to an embodiment will be described in connection with the FIGURE. The organic light-emitting device 10 includes a first electrode 11, an organic layer 15, and a second electrode 19, which are sequentially stacked.

A substrate may be additionally disposed under the first electrode 11 or above the second electrode 19. For use as the substrate, any substrate that is used in general organic light-emitting devices may be used, and the substrate may be a glass substrate or a transparent plastic substrate, each having excellent mechanical strength, thermal stability, transparency, surface smoothness, ease of handling, and water resistance.

The first electrode 11 may be formed by depositing or sputtering a material for forming the first electrode 11 on the substrate. The first electrode 11 may be an anode. The material for forming the first electrode 11 may be a material with a high work function to facilitate hole injection. The first electrode 11 may be a reflective electrode, a semi-reflective electrode, or a transmissive electrode. The material for forming the first electrode may be, for example, indium tin oxide (ITO), indium zinc oxide (IZO), tin oxide (SnO₂), or zinc oxide (ZnO). In one or more embodiments, the material for forming the first electrode 11 may be metal or metal alloy, such as magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In), or magnesium-silver (Mg—Ag).

The first electrode 11 may have a single-layered structure or a multi-layered structure including two or more layers. For example, the first electrode 11 may have a three-layered structure of ITO/Ag/ITO, but the structure of the first electrode 11 is not limited thereto.

The organic layer 15 is disposed on the first electrode 11.

The organic layer 15 may include a hole transport region, an emission layer, and an electron transport region.

The hole transport region may be disposed between the first electrode 11 and the emission layer.

The hole transport region may include a hole injection layer, a hole transport layer, an electron blocking layer, a buffer layer, or any combination thereof.

The hole transport region may include only either a hole injection layer or a hole transport layer. In one or more embodiments, the hole transport region may have a hole injection layer/hole transport layer structure or a hole injection layer/hole transport layer/electron blocking layer structure, which are sequentially stacked in this stated order from the first electrode 11.

When the hole transport region includes a hole injection layer (HIL), the hole injection layer may be formed on the first electrode 11 by using one or more suitable methods, for example, vacuum deposition, spin coating, casting, and/or Langmuir-Blodgett (LB) deposition.

When a hole injection layer is formed by vacuum deposition, the deposition conditions may vary according to a material that is used to form the hole injection layer, and the structure and thermal characteristics of the hole injection layer. For example, the deposition conditions may include a deposition temperature of about 100° C. to about 500° C., a vacuum pressure of about 10⁻⁸ torr to about 10⁻³ torr, and a deposition rate of about 0.01 Å/sec to about 100 Å/sec. However, the deposition conditions are not limited thereto.

When the hole injection layer is formed using spin coating, coating conditions may vary according to the material used to form the hole injection layer, and the structure and thermal properties of the hole injection layer. For example, a coating speed may be from about 2,000 rpm to about 5,000 rpm, and a temperature at which a heat treatment is performed to remove a solvent after coating may be from about 80° C. to about 200° C. However, the coating conditions are not limited thereto.

Conditions for forming a hole transport layer and an electron blocking layer may be understood by referring to conditions for forming the hole injection layer.

The hole transport region may include, for example, m-MTDATA, TDATA, 2-TNATA, NPB, β-NPB, TPD, spiro-TPD, spiro-NPB, methylated-NPB, TAPC, HMTPD, 4,4′,4″-tris(N-carbazolyl)triphenylamine (TCTA), polyaniline/dodecylbenzenesulfonic acid (PANI/DBSA), poly(3,4-ethylenedioxythiophene)/poly(4-styrenesulfonate) (PEDOT/PSS), polyaniline/camphor sulfonic acid (PANI/CSA), polyaniline/poly(4-styrenesulfonate) (PANI/PSS), a compound represented by Formula 201 below, a compound represented by Formula 202 below, or any combination thereof:

In Formula 201, Ar₁₀₁ and Ar₁₀₂ may each independently be a phenylene group, a pentalenylene group, an indenylene group, a naphthylene group, an azulenylene group, a heptalenylene group, an acenaphthylene group, a fluorenylene group, a phenalenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylenylene group, a naphthacenylene group, a picenylene group, a perylenylene group, or a pentacenylene group, each unsubstituted or substituted with deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkyl group, a C₂-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, or any combination thereof.

In Formula 201, xa and xb may each independently be an integer from 0 to 5, or may be 0, 1, or 2. For example, xa may be 1, and xb may be 0, but embodiments of the present disclosure are not limited thereto.

In Formulae 201 and 202, R₁₀₁ to R₁₀₈, R₁₁₁ to R₁₁₉, and R₁₂₁ to R₁₂₄ may each independently be:

-   -   hydrogen, deuterium, —F, —C, —Br, —I, a hydroxyl group, a cyano         group, a nitro group, an amino group, an amidino group, a         hydrazine group, a hydrazone group, a carboxylic acid group or a         salt thereof, a sulfonic acid group or a salt thereof, a         phosphoric acid group or a salt thereof, a C₁-C₁₀ alkyl group         (for example, a methyl group, an ethyl group, a propyl group, a         butyl group, pentyl group, a hexyl group, and the like), or a         C₁-C₁₀ alkoxy group (for example, a methoxy group, an ethoxy         group, a propoxy group, a butoxy group, a pentoxy group, and the         like);     -   a C₁-C₁₀ alkyl group or a C₁-C₁₀ alkoxy group, each substituted         with deuterium, —F, —C, —Br, —I, a hydroxyl group, a cyano         group, a nitro group, an amino group, an amidino group, a         hydrazine group, a hydrazone group, a carboxylic acid group or a         salt thereof, a sulfonic acid group or a salt thereof, a         phosphoric acid group or a salt thereof, or any combination         thereof; or     -   a phenyl group, a naphthyl group, an anthracenyl group, a         fluorenyl group, or a pyrenyl group, each unsubstituted or         substituted with deuterium, —F, —Cl, —Br, —I, a hydroxyl group,         a cyano group, a nitro group, an amino group, an amidino group,         a hydrazine group, a hydrazone group, a carboxylic acid group or         a salt thereof, a sulfonic acid group or a salt thereof, a         phosphoric acid group or a salt thereof, a C₁-C₁₀ alkyl group, a         C₁-C₁₀ alkoxy group, or any combination thereof,     -   but embodiments of the present disclosure are not limited         thereto.

In Formula 201, R₁₀₉ may be a phenyl group, a naphthyl group, an anthracenyl group, or a pyridinyl group, each unsubstituted or substituted with deuterium, —F, —C, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a phenyl group, a naphthyl group, an anthracenyl group, a pyridinyl group, or any combination thereof.

In one embodiment, the compound represented by Formula 201 may be represented by Formula 201A below, but embodiments of the present disclosure are not limited thereto:

Detailed descriptions of R₁₀₁, R₁₁₁, R₁₁₂, and R₁₀₉ in Formula 201A are the same as described above.

For example, the compound represented by Formula 201 and the compound represented by Formula 202 may each include Compounds HT1 to HT20, but are not limited thereto:

A thickness of the hole transport region may be from about 100 Å to about 10,000 Å, for example, about 100 Å to about 1,000 Å. When the hole transport region includes a hole injection layer, a hole transport layer, or any combination thereof, a thickness of the hole injection layer may be in a range of about 100 Å to about 10000 Å, for example, about 100 Å to about 1,000 Å, and a thickness of the hole transport layer may be in a range of about 50 Å to about 2,000 Å, for example about 100 Å to about 1,500 Å. When the thicknesses of the hole transport region, the hole injection layer, and the hole transport layer are within these ranges, satisfactory hole transporting characteristics may be obtained without a substantial increase in driving voltage.

The hole transport region may further include, in addition to these materials, a charge-generation material for the improvement of conductive properties. The charge-generation material may be homogeneously or non-homogeneously dispersed in the hole transport region.

The charge-generation material may be, for example, a p-dopant. The p-dopant may be a quinone derivative, a metal oxide, a cyano group-containing compound, or any combination thereof, but embodiments of the present disclosure are not limited thereto. Non-limiting examples of the p-dopant are a quinone derivative, such as tetracyanoquinodimethane (TCNQ) or 2,3,5,6-tetrafluoro-tetracyano-1,4-benzoquinodimethane (F4-TCNQ); a metal oxide, such as a tungsten oxide or a molybdenum oxide; and a cyano group-containing compound, such as Compound HT-D1 below, but are not limited thereto:

The hole transport region may include a buffer layer.

Also, the buffer layer may compensate for an optical resonance distance according to a wavelength of light emitted from the emission layer, and thus, efficiency of a formed organic light-emitting device may be improved.

Meanwhile, when the hole transport region includes an electron blocking layer, a material for the electron blocking layer may be a material as described for the hole transport region described above, a material for a host to be explained later, or any combination thereof. However, the material for the electron blocking layer is not limited thereto. For example, when the hole transport region includes an electron blocking layer, a material for the electron blocking layer may be mCP, which will be explained later.

An emission layer may be formed on the hole transport region by vacuum deposition, spin coating, casting, LB deposition, or the like. When the emission layer is formed by vacuum deposition or spin coating, the deposition or coating conditions may be similar to those applied in forming the hole injection layer although the deposition or coating conditions may vary according to a compound that is used to form the emission layer.

The emission layer may include a host and a dopant, and the dopant may include the organometallic compound represented by Formula 1.

The host may include TPBi, TBADN, ADN (also referred to as “DNA”), CBP, CDBP, TCP, mCP, one of Compounds H50 to H52, or any combination thereof:

When the organic light-emitting device is a full-color organic light-emitting device, the emission layer may be patterned into a red emission layer, a green emission layer, and/or a blue emission layer. In one or more embodiments, due to a stacked structure including a red emission layer, a green emission layer, and/or a blue emission layer, the emission layer may emit white light.

When the emission layer includes a host and a dopant, an amount of the dopant may be in a range of about 0.01 parts by weight to about 15 parts by weight based on 100 parts by weight of the host, but embodiments of the present disclosure are not limited thereto.

A thickness of the emission layer may be in a range of about 100 Å to about 1,000 Å, for example, about 200 Å to about 600 Å. When the thickness of the emission layer is within this range, excellent light-emission characteristics may be obtained without a substantial increase in driving voltage.

An electron transport region may be disposed on the emission layer.

The electron transport region may include a hole blocking layer, an electron transport layer, an electron injection layer, or any combination thereof.

For example, the electron transport region may have a hole blocking layer/electron transport layer/electron injection layer structure or an electron transport layer/electron injection layer structure, but the structure of the electron transport region is not limited thereto. The electron transport layer may have a single-layered structure or a multi-layered structure including two or more different materials.

Conditions for forming the hole blocking layer, the electron transport layer, and the electron injection layer which constitute the electron transport region may be understood by referring to the conditions for forming the hole injection layer.

When the electron transport region includes a hole blocking layer, the hole blocking layer may include, for example, BCP, Bphen, BAlq, or any combination thereof, but embodiments of the present disclosure are not limited thereto:

A thickness of the hole blocking layer may be from about 20 Å to about 1,000 Å, for example, about 30 Å to about 300 Å. When the thickness of the hole blocking layer is within these ranges, the hole blocking layer may have excellent hole blocking characteristics without a substantial increase in driving voltage.

The electron transport layer may include BCP, Bphen, Alq₃, BAlq, TAZ, NTAZ, or any combination thereof:

In one or more embodiments, the electron transport layer may include one of ET1 to ET25, but embodiments of the present disclosure are not limited thereto:

A thickness of the electron transport layer may be from about 100 Å to about 1,000 Å, for example, about 150 Å to about 500 Å. When the thickness of the electron transport layer is within the range described above, the electron transport layer may have satisfactory electron transport characteristics without a substantial increase in driving voltage.

Also, the electron transport layer may further include, in addition to the materials described above, a metal-containing material.

The metal-containing material may include a Li complex. The Li complex may include, for example, Compound ET-D1 (LiQ), ET-D2, or any combination thereof:

The electron transport region may include an electron injection layer that promotes the flow of electrons from the second electrode 19 thereinto.

The electron injection layer may include LiF, NaCl, CsF, Li₂O, BaO, or any combination thereof.

A thickness of the electron injection layer may be from about 1 Å to about 100 Å, for example, about 3 Å to about 90 Å. When a thickness of the electron injection layer is within these ranges, satisfactory electron injection characteristics may be obtained without substantial increase in driving voltage.

The second electrode 19 is disposed on the organic layer 15. The second electrode 19 may be a cathode. A material for forming the second electrode 19 may be metal, an alloy, an electrically conductive compound, or a combination thereof, which have a relatively low work function. For example, lithium (Li), magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In), or magnesium-silver (Mg—Ag) may be used as the material for forming the second electrode 19. To manufacture a top-emission type light-emitting device, a transmissive electrode formed using ITO or IZO may be used as the second electrode 19.

Hereinbefore, the organic light-emitting device according to an embodiment has been described in connection with the FIGURE.

Another aspect of the present disclosure provides a diagnostic composition including at least one organometallic compound represented by Formula 1.

The organometallic compound represented by Formula 1 provides high luminescence efficiency. Accordingly, a diagnostic composition including the organometallic compound may have high diagnostic efficiency.

The diagnostic composition may be used in various applications including a diagnosis kit, a diagnosis reagent, a biosensor, and a biomarker.

The term “C₁-C₆₀ alkyl group” as used herein refers to a linear or branched saturated aliphatic hydrocarbon monovalent group having 1 to 60 carbon atoms, and examples thereof include a methyl group, an ethyl group, a propyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an isoamyl group, and a hexyl group. The term “C₁-C₆₀ alkylene group” as used herein refers to a divalent group having the same structure as the C₁-C₆₀ alkyl group.

The term “C₁-C₆₀ alkoxy group” as used herein refers to a monovalent group represented by —OA₁₀₁ (wherein A₁₀₁ is the C₁-C₆₀ alkyl group), and examples thereof include a methoxy group, an ethoxy group, and an isopropyloxy group.

The term “C₂-C₆₀ alkenyl group” as used herein refers to a hydrocarbon group having at least one carbon-carbon double bond in the middle or at the terminus of the C₂-C₆₀ alkyl group, and examples thereof include an ethenyl group, a propenyl group, and a butenyl group. The term “C₂-C₆₀ alkenylene group” as used herein refers to a divalent group having the same structure as the C₂-C₆₀ alkenyl group.

The term “C₂-C₆₀ alkynyl group” as used herein refers to a hydrocarbon group having at least one carbon-carbon triple bond in the middle or at the terminus of the C₂-C₆₀ alkyl group, and examples thereof include an ethynyl group, and a propynyl group. The term “C₂-C₆₀ alkynylene group” as used herein refers to a divalent group having the same structure as the C₂-C₆₀ alkynyl group.

The term “C₃-C₁₀ cycloalkyl group” as used herein refers to a monovalent saturated hydrocarbon monocyclic group having 3 to 10 carbon atoms, and non-limiting examples thereof include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group. The term “C₃-C₁₀ cycloalkylene group” as used herein refers to a divalent group having the same structure as the C₃-C₁₀ cycloalkyl group.

The term “C₂-C₁₀ heterocycloalkyl group” as used herein refers to a monovalent saturated monocyclic group having N, O, P, Si, Se, S, or a combination thereof and 2 to 10 carbon atoms as ring-forming atoms, and non-limiting examples thereof include a tetrahydrofuranyl group, and a tetrahydrothiophenyl group. The term “C₂-C₁₀ heterocycloalkylene group” as used herein refers to a divalent group having the same structure as the C₂-C₁₀ heterocycloalkyl group.

The term “C₃-C₁₀ cycloalkenyl group” as used herein refers to a monovalent monocyclic group that has 3 to 10 carbon atoms and at least one carbon-carbon double bond in the ring thereof and no aromaticity, and non-limiting examples thereof include a cyclopentenyl group, a cyclohexenyl group, and a cycloheptenyl group. The term “C₃-C₁₀ cycloalkenylene group” as used herein refers to a divalent group having the same structure as the C₃-C₁₀ cycloalkenyl group.

The term “C₂-C₁₀ heterocycloalkenyl group” as used herein refers to a monovalent monocyclic group that has N, O, P, Si, Se, S, or a combination thereof and 1 to 10 carbon atoms as ring-forming atoms, and a double bond in the ring. Examples of the C₂-C₁₀ heterocycloalkenyl group are a 2,3-dihydrofuranyl group, and a 2,3-dihydrothiophenyl group. The term “C₂-C₁₀ heterocycloalkenylene group” as used herein refers to a divalent group having the same structure as the C₂-C₁₀ heterocycloalkenyl group.

The term “C₆-C₆₀ aryl group” as used herein refers to a monovalent group having a carbocyclic aromatic system having 6 to 60 carbon atoms, and the term “C₆-C₆₀ arylene group” as used herein refers to a divalent group having a carbocyclic aromatic system having 6 to 60 carbon atoms. Non-limiting examples of the C₆-C₆₀ aryl group include a phenyl group, a naphthyl group, an anthracenyl group, a phenanthrenyl group, a pyrenyl group, and a chrysenyl group. When the C₆-C₆₀ aryl group and the C₆-C₆₀ arylene group each include two or more rings, the rings may be fused to each other.

The term “C₁-C₆₀ heteroaryl group” as used herein refers to a monovalent group having a heterocyclic aromatic system that has N, O, P, Si, Se, S, or a combination thereof and 1 to 60 carbon atoms as ring-forming atoms. The term “C₁-C₆₀ heteroarylene group” as used herein refers to a divalent group having a heterocyclic aromatic system that has N, O, P, Si, Se, S, or a combination thereof as ring-forming atoms. Non-limiting examples of the C₁-C₆₀ heteroaryl group include a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, and an isoquinolinyl group. When the C₁-C₆₀ heteroaryl group and the C₁-C₆₀ heteroarylene group each include two or more rings, the rings may be fused to each other.

The term “C₆-C₆₀ aryloxy group” as used herein indicates —OA₁₀₂ (wherein A₁₀₂ is the C₆-C₆₀ aryl group), and the term “C₆-C₆₀ arylthio group” as used herein indicates —SA₁₀₃ (wherein A₁₀₃ is the C₆-C₆₀ aryl group).

The term “monovalent non-aromatic condensed polycyclic group” as used herein refers to a monovalent group (for example, having 8 to 60 carbon atoms) having two or more rings condensed to each other, only carbon atoms as ring-forming atoms, and no aromaticity in its entire molecular structure. Examples of the monovalent non-aromatic condensed polycyclic group include a fluorenyl group. The term “divalent non-aromatic condensed polycyclic group” as used herein refers to a divalent group having the same structure as the monovalent non-aromatic condensed polycyclic group.

The term “monovalent non-aromatic condensed heteropolycyclic group” as used herein refers to a monovalent group (for example, having 2 to 60 carbon atoms) having two or more rings condensed to each other, N, O, P, Si, Se, S, or any combination thereof, other than carbon atoms, as ring-forming atoms, and no aromaticity in its entire molecular structure. Non-limiting examples of the monovalent non-aromatic condensed heteropolycyclic group include a carbazolyl group. The term “divalent non-aromatic condensed heteropolycyclic group” as used herein refers to a divalent group having the same structure as the monovalent non-aromatic condensed heteropolycyclic group.

The term “C₅-C₃₀ carbocyclic group” as used herein refers to a saturated or unsaturated cyclic group having, as ring-forming atoms, 5 to 30 carbon atoms only. The C₅-C₃₀ carbocyclic group may be a monocyclic group or a polycyclic group.

The term “C₂-C₃₀ heterocyclic group” as used herein refers to a saturated or unsaturated cyclic group having, N, O, Si, P, Se, S, or any combination thereof and 2 to 30 carbon atoms as ring-forming atoms. The C₂-C₃₀ heterocyclic group may be a monocyclic group or a polycyclic group.

A substituent(s) of the substituted C₅-C₃₀ carbocyclic group, the substituted C₂-C₃₀ heterocyclic group, the substituted C₁-C₆₀ alkyl group, the substituted C₂-C₆₀ alkenyl group, the substituted C₂-C₆₀ alkynyl group, the substituted C₁-C₆₀ alkoxy group, the substituted C₃-C₁₀ cycloalkyl group, the substituted C₂-C₁₀ heterocycloalkyl group, the substituted C₃-C₁₀ cycloalkenyl group, the substituted C₂-C₁₀ heterocycloalkenyl group, the substituted C₆-C₆₀ aryl group, the substituted C₆-C₆₀ aryloxy group, the substituted C₆-C₆₀ arylthio group, the substituted C₁-C₆₀ heteroaryl group, the substituted monovalent non-aromatic condensed polycyclic group, and the substituted monovalent non-aromatic condensed heteropolycyclic group may be:

-   -   deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H,         —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino         group, an amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, or a C₁-C₆₀ alkoxy group;     -   a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, or a C₁-C₆₀ alkoxy group, each substituted with         deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H,         —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino         group, an amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, a monovalent non-aromatic condensed         heteropolycyclic group, —N(Q₁₁)(Q₁₂), —Si(Q₁₃)(Q₁₄)(Q₁₅),         —B(Q₁₆)(Q₁₇), —P(═O)(Q₁₈)(Q₁₉), or any combination thereof;     -   a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, or a monovalent non-aromatic         condensed heteropolycyclic group;     -   a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic         condensed polycyclic group, or a monovalent non-aromatic         condensed heteropolycyclic group, each substituted with         deuterium, —F, —C, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H,         —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino         group, an amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a         C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a         C₂-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀         aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl         group, a monovalent non-aromatic condensed polycyclic group, a         monovalent non-aromatic condensed heteropolycyclic group,         —N(Q₂₁)(Q₂₂), —Si(Q₂₃)(Q₂₄)(Q₂₅), —B(Q₂₆)(Q₂₇),         —P(═O)(Q₂₈)(Q₂₉), or any combination thereof;     -   —N(Q₃₁)(Q₃₂), —Si(Q₃₃)(Q₃₄)(Q₃₅), —B(Q₃₆)(Q₃₇), or         —P(═O)(Q₃₈)(Q₃₉); or     -   any combination thereof.

In the present specification, Q₁ to Q₉, Q₁₁ to Q₁₉, Q₂₁ to Q₂₉, and Q₃₁ to Q₃₉ may each independently be hydrogen, deuterium, —F, —C, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryl group substituted with a C₁-C₆₀ alkyl group, a C₆-C₆₀ aryl group or any combination thereof, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, or any combination thereof.

Hereinafter, a compound and an organic light-emitting device according to embodiments are described in detail with reference to Synthesis Example and Examples. However, the organic light-emitting device is not limited thereto. The wording “B was used instead of A” used in describing Synthesis Examples means that an amount of A used was identical to an amount of B used, in terms of a molar equivalent.

EXAMPLES Synthesis Example 1 (Compound 1)

Synthesis of Intermediate L1

5-chloro-2-phenylfuro[2,3-c]pyridine (2.55 g, 11.1 mmol), phenylboronic acid (2.603 g, 16.64 mmol), Pd(PPh₃)₄ (1.03 g, 0.89 mmol), and K₂CO₃ (3.83 g, 27.7 mmol) were mixed with 60 mL of tetrahydrofuran and 30 mL of distilled water, stirred at a temperature of 90° C. for 18 hours, and then cooled to room temperature. The reaction mixture was extracted with ethyl acetate, dried by using anhydrous magnesium sulfate (MgSO₄), and filtered to obtain a filtrate. The filtrate was concentrated under vacuum to obtain a residue. The residue was purified by column chromatography using ethyl acetate:hexane=1:2 (V/V) as an eluent to obtain Intermediate L1 (2.90 g, 83%).

LC-MS m/z=272.31 (M+H)⁺.

Synthesis of Intermediate L1-dimer

Intermediate L1 (1.99 g, 7.32 mmol) and Iridium chloride hydrate (1.15 g, 3.25 mmol) were mixed with 21 mL of 2-ethoxy ethanol and 7 mL of distilled water, stirred at a temperature of 120° C. for 24 hours under reflux, and then cooled to room temperature. A solid obtained therefrom was filtered, and the filtered solid was sufficiently washed in the order of water/methanol/hexane. The solid was dried in a vacuum oven to obtain Intermediate L1-dimer (1.95 g, 78%). The obtained compound was used in a next reaction without additional purification.

Synthesis of Compound 1

30 mL of 2-ethoxy ethanol was added to Intermediate L1-dimer (1.94 g, 1.26 mmol), acetyl acetone (1.26 g, 12.6 mmol), and Na₂CO₃ (1.33 g, 12.6 mmol), and stirred at room temperature for 12 hours. The reaction mixture was extracted using ethyl acetate, dried by using anhydrous magnesium sulfate (MgSO₄), and filtered to obtain a filtrate. The filtrate was concentrated under vacuum to obtain a residue. The residue was purified by column chromatography using methylene chloride:hexane=1:4 (V/V) as an eluent to obtain Compound 1 (0.453 g, 22%). The obtained compound was identified by Mass Spectrometry (MS) and HPLC analysis.

HRMS(MALDI-TOF) calcd for C₄₃H₃₁IrN₂O₄: m/z 832.1913, Found: 832.1912.

Synthesis Example 2 (Compound 16)

Synthesis of Intermediate L16

5-chloro-2-phenylfuro[2,3-c]pyridine (2.69 g, 11.71 mmol), (3,5-dimethylphenyl)boronic acid (2.64 g, 17.56 mmol), Pd(PPh₃)₄ (1.08 g, 0.94 mmol), and K₂CO₃ (4.05 g, 29.3 mmol) were mixed with 60 mL of tetrahydrofuran and 30 mL of distilled water, stirred at a temperature of 90° C. for 18 hours, and then cooled to room temperature. The reaction mixture was extracted using ethyl acetate, dried by using anhydrous magnesium sulfate (MgSO₄), and filtered to obtain a filtrate. The filtrate was concentrated under vacuum to obtain a residue. The residue was purified by column chromatography using ethyl acetate:hexane=1:2 (V/V) as an eluent to obtain Intermediate L16 (3.02 g, 86%).

LC-MS m/z=300.13 (M+H)⁺.

Synthesis of Intermediate L16-dimer

Intermediate L16 (2.04 g, 6.82 mmol) and iridium chloride hydrate (1.07 g, 3.03 mmol) were mixed with 21 mL of 2-ethoxy ethanol and 7 mL of distilled water, stirred at a temperature of 120° C. for 24 hours under reflux, and then cooled to room temperature. A solid obtained therefrom was filtered, and the filtered solid sufficiently washed in the order of water/methanol/hexane. The solid was dried in a vacuum oven to obtain Intermediate L16-dimer (2.17 g, 87%). The obtained compound was used in a next reaction without additional purification.

Synthesis of Compound 16

30 mL of 2-ethoxy ethanol was added to Intermediate L16-dimer (2.14 g, 1.29 mmol), acetyl acetone (1.29 g, 12.9 mmol), and Na₂CO₃ (1.37 g, 12.9 mmol), and stirred at room temperature for 12 hours. The reaction mixture was extracted using ethyl acetate, dried by using anhydrous magnesium sulfate (MgSO₄), and filtered to obtain a filtrate. The filtrate was concentrated under vacuum to obtain a residue. The residue was purified by column chromatography using methylene chloride:hexane=1:4 (V/V) as an eluent to obtain Compound 16 (0.47 g, 20%). The obtained compound was identified by MS and HPLC analysis.

HRMS(MALDI-TOF) calcd for C₄₇H₃₉IrN₂O₄: m/z 888.2539, Found: 888.2541.

Synthesis Example 3 (Compound 31)

Synthesis of Intermediate L31

Intermediate L31 (2.54 g, 85%) was obtained in the same manner as in Synthesis of Intermediate L1 of Synthesis Example 1, except that diphenyl 3-boronic acid ([1,1′-biphenyl]-3-ylboronic acid) (2.57 g, 12.9 mmol) was used instead of phenylboronic acid (2.603 g, 16.64 mmol).

LC-MS m/z=348 (M+H)⁺.

Synthesis of Intermediate L31-dimer

Intermediate L31-dimer (1.89 g, 76%) was obtained in the same manner as in Synthesis of Intermediate L1-dimer of Synthesis Example 1, except that Intermediate L31 (2.12 g, 6.11 mmol) was used instead of Intermediate L1.

Synthesis of Compound 31

Compound 31 (0.45 g, 23%) was obtained in the same manner as in Synthesis of Compound 1 of Synthesis Example 1, except that Intermediate L31-dimer (1.87 g, 1.25 mmol) was used instead of Intermediate L1-dimer. The obtained compound was identified by MS and HPLC analysis.

HRMS(MALDI-TOF) calcd for C₅₅H₃₉IrN₂O₄: m/z 984.2539, Found: 984.2539.

Synthesis Example 4 (Compound 236)

Synthesis of Intermediate L236

Intermediate L236 (2.54 g, 85%) was obtained in the same manner as in Synthesis of Intermediate L16 of Synthesis Example 2, except that 5-chloro-2-phenylthieno[2,3-c]pyridine (2.34 g, 9.51 mmol) was used instead of 5-chloro-2-phenylfuro[2,3-c]pyridine (2.69 g, 11.71 mmol).

LC-MS m/z=316 (M+H)⁺.

Synthesis of Intermediate L236-dimer

Intermediate L236-dimer (2.11 g, 84%) was obtained in the same manner as in Synthesis of Intermediate L16-dimer of Synthesis Example 2, except that Intermediate L236 (2.07 g, 6.57 mmol) was used instead of Intermediate L16.

Synthesis of Compound 236

Compound 236 (0.41 g, 19%) was obtained in the same manner as in Synthesis of Compound 16 of Synthesis Example 2, except that Intermediate L236-dimer (2.05 g, 1.20 mmol) was used instead of Intermediate L16-dimer. The obtained compound was identified by MS and HPLC analysis.

HRMS (MALDI-TOF) calcd for C₄₇H₃₉IrN₂O₂ S₂: m/z 920.2082, Found: 920.2080.

Synthesis Example 5 (Compound 346)

Synthesis of Intermediate L346

Intermediate L346 (2.67 g, 87%) was obtained in the same manner as in Synthesis of Intermediate L16 of Synthesis Example 2, except that 6-chloro-2-phenylthieno[3,2-c]pyridine (2.34 g, 9.51 mmol) was used instead of 5-chloro-2-phenylfuro[2,3-c]pyridine (2.69 g, 11.71 mmol).

LC-MS m/z=316 (M+H)⁺.

Synthesis of Intermediate L346-dimer

Intermediate L346-dimer (2.25 g, 80%) was obtained in the same manner as in Synthesis of Intermediate L16-dimer of Synthesis Example 2, except that Intermediate L346 (2.32 g, 7.36 mmol) was used instead of Intermediate L16.

Synthesis of Compound 346

Compound 346 (0.526 g, 23%) was obtained in the same manner as in Synthesis of Compound 16 of Synthesis Example 2, except that Intermediate L346-dimer (2.14 g, 1.25 mmol) was used instead of Intermediate L16-dimer. The obtained compound was identified by MS and HPLC analysis.

HRMS (MALDI-TOF) calcd for C₄₇H₃₉IrN₂O₂ S₂: m/z 920.2082, Found: 920.2081.

Synthesis Example 6 (Compound 468)

Synthesis of Intermediate L468

Intermediate L468 (3.02 g, 74%) was obtained in the same manner as in Synthesis of Intermediate L1 of Synthesis Example 1, except that 6-chloro-2-phenylthieno[3,2-c]pyridine (3.51 g, 14.3 mmol) was used instead of 5-chloro-2-phenylfuro[2,3-c]pyridine (2.69 g, 11.71 mmol).

Synthesis of Intermediate L468-dimer

Intermediate L468-dimer (2.11 g, 96%) was obtained in the same manner as in Synthesis of Intermediate L1-dimer of Synthesis Example 1, except that Intermediate L468 (1.78 g, 6.19 mmol) was used instead of Intermediate L1.

Synthesis of Intermediate L468-dimer-OTf

60 mL of methylene chloride (MC) was mixed with Intermediate L468-dimer (1.97 g, 1.23 mmol), and AgOTf (0.631 g, 2.46 mmol) was dissolved in 20 mL of methanol and added thereto. Then, the reaction proceeded with stirring at room temperature for 18 hours in a state in which light was blocked by an aluminum foil. The reaction mixture was filtered through celite, and a filtrate was concentrated under vacuum to obtain Intermediate L468-dimer-OTf. Intermediate L468-dimer-OTf was used in a next reaction without additional purification.

Synthesis of Compound 468

Intermediate L468-dimer-OTf (2.23 g, 2.28 mmol) and 2-phenylpyridine (0.39 g, 2.51 mmol) were mixed with 100 mL of ethanol, stirred for 18 hours under reflux, and then cooled. A mixture obtained therefrom was filtered to obtain a solid. The solid was sufficiently washed with ethanol and hexane, and column chromatography using MC:hexane=40:60 (V/V) as an eluent was performed thereon to obtain Compound 468 (0.32 g, 19%). The obtained compound was identified by MS and HPLC analysis.

HRMS (MALDI-TOF) calcd for C₄₉H₃₂IrN₃S₂: m/z 919.1667, Found: 919.1666.

Synthesis Example 7 (Compound 469)

Synthesis of Intermediate 469(1)

2-phenylpyridine (14.66 g, 94.44 mmol) and Iridium chloride (14.80 g, 41.97 mmol) were mixed with 210 mL of 2-ethoxy ethanol and 70 mL of distilled water, stirred for 24 hours under reflux, and then cooled to room temperature. A solid obtained therefrom was filtered, and sufficiently washed in the order of water/methanol/hexane. The solid was dried in a vacuum oven to obtain Intermediate 469(1) (19.5 g, 87%).

Synthesis of Intermediate 469(2)

60 mL of MC was mixed with Intermediate 469(1) (1.88 g, 1.75 mmol), and AgOTf (0.90 g, 3.50 mmol) was dissolved in 20 mL of methanol and added thereto. Then, the reaction proceeded while stirring at room temperature for 18 hours in a state in which light was blocked by an aluminum foil. The reaction mixture was filtered through celite, and a filtrate was concentrated under vacuum to obtain Intermediate L469(2). Intermediate L469(2) was used in a next reaction without additional purification.

Synthesis of Compound 469

Intermediate 469(2) (1.27 g, 1.78 mmol) and Intermediate L468 (0.562 g, 1.96 mmol) were mixed with 40 mL of ethanol, stirred for 18 hours under reflux, and then cooled.

A mixture obtained therefrom was filtered to obtain a solid. The solid was sufficiently washed with ethanol and hexane, and column chromatography using MC:hexane=40:60 (V/V) as an eluent was performed thereon to obtain Compound 469 (0.31 g, 22%). The obtained compound was identified by MS and HPLC analysis.

HRMS (MALDI-TOF) calcd for C₄₁H₂₈IrN₃S: m/z 787.1633, Found: 787.1633.

Evaluation Example 1: Evaluation of Radiative Decay Rate

CBP and Compound 1 were co-deposited at a weight ratio of 9:1 under a vacuum pressure of 10-7 torr to manufacture a film having a thickness of 40 nm.

A PL spectrum of the film was evaluated at room temperature by using a PicoQuant TRPL measurement system FluoTime 300 and a PicoQuant pumping source PLS340 (excitation wavelength=340 nm, spectral width=20 nm), a wavelength of a main peak of the spectrum was determined, and PLS340 repeatedly measured the number of photons emitted from the film at the wavelength of the main peak due to a photon pulse (pulse width=500 ps) applied to the film according to time based on time-correlated single photon counting (TCSPC), thereby obtaining a sufficiently fittable TRPL curve. A decay time T_(decay) of the film was obtained by fitting one or more exponential decay functions to the result obtained therefrom. The function used for fitting is expressed by Equation 10, and the greatest value among the values obtained from each exponential decay function used for fitting was taken as T_(decay). At this time, a baseline or background signal curve was obtained by repeating the same measurement once more for the same measurement time as the measurement time for obtaining the TRPL curve in a dark state (a state in which a pumping signal applied to the predetermined film was blocked), and the baseline or background signal curve was used for fitting as a baseline.

$\begin{matrix} {{f(t)} = {\sum\limits_{i = 1}^{n}{A_{i}\mspace{14mu}\exp\mspace{11mu}\left( {{- t}\text{/}T_{{decay},i}} \right)}}} & {{Equation}\mspace{14mu} 10} \end{matrix}$

Then, the quantum efficiency of the film was measured by using a Hamamatsu Quantaurus-QY Absolute PL quantum yield spectrometer (provided with a xenon light source, a monochromator, a photonic multichannel analyzer, and an integrating sphere and using PLQY measurement software (Hamamatsu Photonics, Ltd., Shizuoka, Japan)). Upon measurement of the quantum efficiency, the excitation wavelength was measured while scanning from 320 nm to 380 nm at an interval of 10 nm, and the greatest value was taken as the quantum efficiency (ϕ).

The radiative decay rate (k_(r)) of Compound 1 was obtained by substituting T_(decay) and ϕ into Equation 11, and results thereof are shown in Table 2. k _(r) =ϕ/T _(decay)  Equation 11

The measurement of the radiative decay rate was repeated on Compounds 16, 31, 236, 346, 468, 469, A1, A2, B, C1, C2, and D, and results thereof are shown in Table 2.

TABLE 2 Compound No. Radiative decay rate (s⁻¹) 1 6.70 × 10⁵ 16 8.94 × 10⁵ 31 8.26 × 10⁵ 236 1.36 × 10⁶ 346 1.17 × 10⁶ 468 6.46 × 10⁵ 469 5.56 × 10⁵ A1 3.17 × 10⁵ A2 3.32 × 10⁵ B 4.62 × 10⁵ C1 1.27 × 10⁵ C2 2.93 × 10⁵ D 3.25 × 10⁵

From Table 2, it is confirmed that Compounds 1, 16, 31, 236, 346, 468, and 469 have high radiative decay rates, as compared with those of Compounds A1, A2, B, C1, C2, and D.

Example 1

As an anode, a glass substrate, on which ITO/Ag/ITO were deposited to thicknesses of 70 Å/1,000 Å/70 Å, was cut to a size of 50 mm×50 mm×0.5 mm, sonicated with isopropyl alcohol and pure water each for 5 minutes, and then cleaned by exposure to ultraviolet rays and ozone for 30 minutes. Then, the glass substrate was provided to a vacuum deposition apparatus.

2-TNATA was vacuum-deposited on the anode to form a hole injection layer having a thickness of 600 Å, and 4,4′-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (NPB) was vacuum-deposited on the hole injection layer to form a hole transport layer having a thickness of 1,350 Å.

Then, CBP (host) and Compound 1 (dopant) were co-deposited on the hole transport layer at a weight ratio of 98:2 to form an emission layer having a thickness of 400 Å.

Then, BCP was vacuum-deposited on the emission layer to form a hole blocking layer having a thickness of 50 Å, Alq3 was vacuum-deposited on the hole blocking layer to form an electron transport layer having a thickness of 350 Å, LiF was vacuum-deposited on the electron transport layer to form an electron injection layer having a thickness of 10 Å, and Mg and Ag were co-deposited on the electron injection layer at a weight ratio of 90:10 to form a cathode having a thickness of 120 Å, thereby completing the manufacture of an organic light-emitting device (which emits red light).

Examples 2 to 7 and Comparative Examples A1, A2, B, C1, C2, and D

Organic light-emitting devices were manufactured in the same manner as in Example 1, except that Compounds shown in Table 3 were each used instead of Compound 1 as a dopant informing an emission layer.

Evaluation Example 2: Evaluation of Characteristics of Organic Light-Emitting Devices

The driving voltage, maximum value of external quantum efficiency (Max EQE), roll-off ratio, maximum emission wavelength of main peak of EL spectrum, and lifespan (T₉₇) of the organic light-emitting devices manufactured according to Examples 1 to 7 and Comparative Examples A1, A2, B, C1, C2, and D were evaluated, and results thereof are shown in Table 3. A current-voltage meter (Keithley 2400) and a luminance meter (Minolta Cs-1000A) were used as the evaluation devices, and the lifespan (T₉₇) (at 3,500 nit) indicates an amount of time that lapsed when luminance was 97% of initial luminance (100%). The roll-off ratio was calculated by Equation 20: Roll off ratio={1−(efficiency(at 3,500 nit)/maximum luminescence efficiency)}×100%  Equation 20

TABLE 3 Compound Maximum LT₉₇ No. of Roll- emission (hr) dopant in Driving Max Off wave- (at emission voltage EQE ratio length 3,500 layer (V) (%) (%) (nm) nit) Example 1 1 4.0 28.4 8 524 273 Example 2 16 3.7 30.1 9 558 205 Example 3 31 3.8 26.6 6 533 155 Example 4 236 3.5 31.9 7 582 320 Example 5 346 3.7 31.7 10 565 232 Example 6 468 3.6 28.4 9 540 253 Example 7 469 4.0 26.8 8 538 212 Comparative A1 5.2 24.8 13 530 120 Example A1 Comparative A2 4.8 24.0 11 540 65 Example A2 Comparative B 4.3 26.0 12 580 60 Example B Comparative C1 4.8 21.8 12 515 108 Example Cl Comparative C2 5.4 22.9 15 510 34 Example C2 Comparative D 4.6 22.0 12 552 33 Example D

From Table 3, it is confirmed that the organic light-emitting devices of Examples 1 to 7 emit red light and have improved driving voltage, improved external quantum efficiency, improved roll-off ratio, and improved lifespan characteristics, as compared with those of the organic light-emitting devices of Comparative Examples A1, A2, B, C1, C2, and D.

Since the organometallic compound represented by Formula 1 has a high radiative decay rate, an electronic device, for example, an organic light-emitting device, which includes the organometallic compound represented by Formula 1, may have improved driving voltage, improved external quantum luminescence efficiency, improved roll-off ratio, and improved lifespan characteristics. In addition, since the organometallic compound represented by Formula 1 has excellent phosphorescent luminescent characteristics, a diagnostic composition having high diagnostic efficiency may be provided by using the organometallic compound.

It should be understood that embodiments described herein should be considered in a descriptive sense only and not for purposes of limitation. Descriptions of features or aspects within each embodiment should typically be considered as available for other similar features or aspects in other embodiments.

While one or more embodiments have been described with reference to the FIGURES, it will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the spirit and scope as defined by the following claims. 

What is claimed is:
 1. An organometallic compound represented by Formula 1: M(L ₁)n ₁(L ₂)n ₂,  Formula 1 wherein, in Formula 1, M is a transition metal, L₁ is a ligand represented by Formula 2, n1 is 1, 2, or 3, wherein, when n1 is 2 or more, two or more L₁ are identical to or different from each other, L₂ is a monodentate ligand, a bidentate ligand, a tridentate ligand, or a tetradentate ligand, n2 is 0, 1, 2, 3, or 4, wherein, when n2 is 2 or more, two or more L₂ are identical to or different from each other, and L₁ and L₂ are different from each other:

wherein, in Formula 2, X₁ is C, N, Si, or P, X₂₁ is C, ring CY₁ and ring CY₂₁ are each independently a C₅-C₃₀ carbocyclic group or a C₂-C₃₀ heterocyclic group, i) X₂ is O, S, or Se, and X₃ is C(R₂); or ii) X₂ is C(R₂), and X₃ is O, S, or Se, X₄ is C(R₄), X₅ is C(R₅), R₁, R₂, R₄, R₅, and R₂₁ are each independently hydrogen, deuterium, —F, —Cl, —Br, —I, —SF₅, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₂-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₂-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), —P(═O)(Q₈)(Q₉) or —P(Q₅)(Q₉), a1 and a21 are each independently an integer from 0 to 20, ring CY₁ and R₂ are not linked to each other, and R₁ and R₂ are not linked to each other, L₁₁ is a C₅-C₃₀ carbocyclic group that is unsubstituted or substituted with at least one R_(10a) or a C₂-C₃₀ heterocyclic group that is unsubstituted or substituted with at least one R_(10a), b11 is 0, wherein, when b11 is 0, a group represented by *-(L₁₁)b₁₁-*′ is a single bond, two of a plurality of neighboring R₂₁ are optionally linked to form a C₅-C₃₀ carbocyclic group that is unsubstituted or substituted with at least one R_(10a) or a C₂-C₃₀ heterocyclic group that is unsubstituted or substituted with at least one R_(10a), R_(10a) is the same as defined in connection with R₂₁, * and *′ each indicate a binding site to M in Formula 1, a substituent of the substituted C₅-C₃₀ carbocyclic group, the substituted C₂-C₃₀ heterocyclic group, the substituted C₁-C₆₀ alkyl group, the substituted C₂-C₆₀ alkenyl group, the substituted C₂-C₆₀ alkynyl group, the substituted C₁-C₆₀ alkoxy group, the substituted C₃-C₁₀ cycloalkyl group, the substituted C₂-C₁₀ heterocycloalkyl group, the substituted C₃-C₁₀ cycloalkenyl group, the substituted C₂-C₁₀ heterocycloalkenyl group, the substituted C₆-C₆₀ aryl group, the substituted C₆-C₆₀ aryloxy group, the substituted C₆-C₆₀ arylthio group, the substituted C₁-C₆₀ heteroaryl group, the substituted monovalent non-aromatic condensed polycyclic group, and the substituted monovalent non-aromatic condensed heteropolycyclic group is: deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, or a C₁-C₆₀ alkoxy group; a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, or a C₁-C₆₀ alkoxy group, each substituted with deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —N(Q₁₁)(Q₁₂), —Si(Q₁₃)(Q₁₄)(Q₁₅), —B(Q₁₆)(Q₁₇), —P(═O)(Q₁₈)(Q₁₉), or any combination thereof; a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, or a monovalent non-aromatic condensed heteropolycyclic group; a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, or a monovalent non-aromatic condensed heteropolycyclic group, each substituted with deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropoly cyclic group, —N(Q₂₁)(Q₂₂), —Si(Q₂₃)(Q₂₄)(Q₂₅), —B(Q₂₆)(Q₂₇), —P(═O)(Q₂₈)(Q₂₉), or any combination thereof; —N(Q₃₁)(Q₃₂), —Si(Q₃₃)(Q₃₄)(Q₃₅), —B(Q₃₆)(Q₃₇), or —P(═O)(Q₃₈)(Q₃₉); or any combination thereof, and Q₁ to Q₉, Q₁₁ to Q₁₉, Q₂₁ to Q₂₉, and Q₃₁ to Q₃₉ are each independently hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryl group substituted with a C₁-C₆₀ alkyl group, a C₆-C₆₀ aryl group, or any combination thereof, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, or a monovalent non-aromatic condensed heteropolycyclic group.
 2. The organometallic compound of claim 1, wherein M is Ir, and the sum of n1 and n2 is 3; or M is Os, and the sum of n1 and n2 is 4; or M is Pt, and the sum of n1 and n2 is
 2. 3. The organometallic compound of claim 1, wherein, ring CY₁ and ring CY₂₁ are each independently a cyclopentene group, a cyclohexene group, a benzene group, a naphthalene group, an anthracene group, a phenanthrene group, a triphenylene group, a pyrene group, a chrysene group, a cyclopentadiene group, a 1,2,3,4-tetrahydronaphthalene group, a thiophene group, a furan group, an indole group, a benzoborole group, a benzophosphole group, an indene group, a benzosilole group, a benzogermole group, a benzothiophene group, a benzoselenophene group, a benzofuran group, a carbazole group, a dibenzoborole group, a dibenzophosphole group, a fluorene group, a dibenzosilole group, a dibenzogermole group, a dibenzothiophene group, a dibenzoselenophene group, a dibenzofuran group, a dibenzothiophene 5-oxide group, a 9H-fluorene-9-one group, a dibenzothiophene 5,5-dioxide group, an azaindole group, an azabenzoborole group, an azabenzophosphole group, an azaindene group, an azabenzosilole group, an azabenzogermole group, an azabenzothiophene group, an azabenzoselenophene group, an azabenzofuran group, an azacarbazole group, an azadibenzoborole group, an azadibenzophosphole group, an azafluorene group, an azadibenzosilole group, an azadibenzogermole group, an azadibenzothiophene group, an azadibenzoselenophene group, an azadibenzofuran group, an azadibenzothiophene 5-oxide group, an aza-9H-fluorene-9-one group, an azadibenzothiophene 5,5-dioxide group, a pyridine group, a pyrimidine group, a pyrazine group, a pyridazine group, a triazine group, a quinoline group, an isoquinoline group, a quinoxaline group, a quinazoline group, a phenanthroline group, a pyrrole group, a pyrazole group, an imidazole group, a triazole group, an oxazole group, an isoxazole group, a thiazole group, an isothiazole group, an oxadiazole group, a thiadiazole group, a benzopyrazole group, a benzimidazole group, a benzoxazole group, a benzothiazole group, a benzoxadiazole group, a benzothiadiazole group, a 5,6,7,8-tetrahydroisoquinoline group, or a 5,6,7,8-tetrahydroquinoline group.
 4. The organometallic compound of claim 1, wherein R₁, R₂, R₄, R₅, R₂₁, and R_(10a) are each independently: hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, —SF₅, a C₁-C₂₀ alkyl group, or a C₁-C₂₀ alkoxy group; a C₁-C₂₀ alkyl group or a C₁-C₂₀ alkoxy group, each substituted with deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₁₀ alkyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an adamantyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a bicyclo[1.1.1]pentyl group, a bicyclo[2.1.1]hexyl group, a bicyclo[2.2.1]heptyl group, a bicyclo[2.2.2]octyl group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a pyridinyl group, a pyrimidinyl group, or any combination thereof; a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an adamantyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a cyclooctenyl group, a bicyclo[1.1.1]pentyl group, a bicyclo[2.1.1]hexyl group, a bicyclo[2.2.1]heptyl group, a bicyclo[2.2.2]octyl group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthrolinyl group, a benzimidazolyl group, a benzofuranyl group, a benzothiophenyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, an imidazopyridinyl group, or an imidazopyrimidinyl group, each unsubstituted or substituted with deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an adamantyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a cyclooctenyl group, a bicyclo[1.1.1]pentyl group, a bicyclo[2.1.1]hexyl group, a bicyclo[2.2.1]heptyl group, a bicyclo[2.2.2]octyl group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthrolinyl group, a benzimidazolyl group, a benzofuranyl group, a benzothiophenyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, an imidazopyridinyl group, an imidazopyrimidinyl group, —Si(Q₃₃)(Q₃₄)(Q₃₅), or any combination thereof; or N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), —P(═O)(Q₈)(Q₉), or —P(Q₈)(Q₉), and Q₁ to Q₉ and Q₃₃ to Q₃₅ are each independently: —CH₃, —CD₃, —CD₂H, —CDH₂, —CH₂CH₃, —CH₂CD₃, —CH₂CD₂H, —CH₂CDH₂, —CHDCH₃, —CHDCD₂H, —CHDCDH₂, —CHDCD₃, —CD₂CD₃, —CD₂CD₂H, or —CD₂CDH₂; or an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an isopentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, or a naphthyl group, each unsubstituted or substituted with deuterium, a C₁-C₁₀ alkyl group, a phenyl group, or any combination thereof.
 5. The organometallic compound of claim 1, wherein a group represented by

in Formula 2 is a C₃-C₁₀ cycloalkenyl group, a C₂-C₁₀ heterocycloalkenyl group, a C₆-C₃₀ aryl group, a C₂-C₃₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, or a monovalent non-aromatic condensed heteropoly cyclic group, each unsubstituted or substituted with R₁ in the number of a1, in Formula 2, R₁ and R₂ are each independently: hydrogen, deuterium, —F, —Cl, —Br, —I, a cyano group, or —SF₅; or a C₁-C₆₀ alkyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₂-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, or C₂-C₁₀ heterocycloalkenyl group, each unsubstituted or substituted with deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a cyano group, a C₁-C₂₀ alkyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an adamantyl group, a norbornyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a phenyl group, a biphenyl group, a naphthyl group, a pyridinyl group, a pyrimidinyl group, or any combination thereof, and a1 is an integer from 0 to
 10. 6. The organometallic compound of claim 1, wherein a group represented by

in Formula 2 is a phenyl group, a biphenyl group, a naphthyl group, a fluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthrolinyl group, a benzimidazolyl group, a benzofuranyl group, a benzothiophenyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, an imidazopyridinyl group, or an imidazopyrimidinyl group, each unsubstituted or substituted with R₁ in the number of a1, in Formula 2, R₁ and R₂ are each independently: hydrogen, deuterium, —F, —Cl, —Br, —I, a cyano group, or —SF₅; or a methyl group, an ethyl group, a propyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an isopentyl group, a sec-pentyl group, a tert-pentyl group, an n-hexyl group, an isohexyl group, a sec-hexyl group, a tert-hexyl group, an n-heptyl group, an isoheptyl group, a sec-heptyl group, a tert-heptyl group, an n-octyl group, an isooctyl group, a sec-octyl group, a tert-octyl group, an n-nonanyl group, an isononanyl group, a sec-nonanyl group, a tert-nonanyl group, an n-decanyl group, an isodecanyl group, a sec-decanyl group, a tert-decanyl group, a C₁-C₁₀ alkoxy, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an adamantyl group, a norbornyl group, a norbomenyl group, a cyclopentenyl group, a cyclohexenyl group, or a cycloheptenyl group, each unsubstituted or substituted with deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a cyano group, a C₁-C₂₀ alkyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an adamantyl group, a norbornyl group, a norbomenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a phenyl group, a biphenyl group, a naphthyl group, a pyridinyl group, a pyrimidinyl group, or any combination thereof, and a1 is an integer from 0 to
 5. 7. The organometallic compound of claim 1, wherein a group represented by

is a group represented by one of Formulae 10-13(1) to 10-13(18) and 10-13:

wherein, in Formulae 10-13(1) to 10-13(18) and 10-13, R_(1a) to R_(1e) are each independently the same as defined in connection with R₁ in claim 1, wherein R_(1a) to R_(1e) are each not hydrogen, and * indicates a binding site to a neighboring atom.
 8. The organometallic compound of claim 1, wherein a group represented by

in Formula 2 is a group represented by one of Formulae CY21-1 to CY21-25:

wherein, in Formulae CY21-1 to CY21-25, X₂₁ and R₂₁ are each independently the same as described in claim 1, X₂₂ is C(R₂₂)(R₂₃), N(R₂₂), O, S, or Si(R₂₂)(R₂₃), R₂₂ to R₂₉ are each independently the same as defined in connection with R₂₁ in claim 1, a26 is an integer from 0 to 6, a24 is an integer from 0 to 4, a23 is an integer from 0 to 3, a22 is an integer from 0 to 2, *″ indicates a binding site to a carbon atom of a neighboring 6-membered ring in Formula 2, and * indicates a binding site to M in Formula
 1. 9. The organometallic compound of claim 8, wherein a group represented by

in Formula 2 is a group represented by one of Formulae CY21(1) to CY21(56) or a group represented by one of Formulae CY21-20 to CY21-25:

wherein, in Formulae CY21(1) to CY21(56), X₂₁ and R₂₁ are each independently the same as described in claim 1, R_(21a) to R_(21d) are each independently the same as defined in connection with R₂₁ in claim 1, wherein R₂₁ and R_(21a) to R_(21d) are each not hydrogen, *″ indicates a binding site to a carbon atom of a neighboring 6-membered ring in Formula 2, and * indicates a binding site to M in Formula
 1. 10. The organometallic compound of claim 1, wherein L₁ is a ligand represented by Formula 2A or 2B:

wherein, in Formulae 2A and 2B, X₁, X₂₁, ring CY₁, ring CY₂₁, X₄, X₅, R₁, R₂, R₂₁, a1, a21, L₁₁, b11, *, and *′ are each independently the same as described in claim 1, wherein X₂ and X₃ are each independently O, S, or Se.
 11. The organometallic compound of claim 1, wherein, in Formula 1, L₂ is a bidentate ligand linked to M in Formula 1 via O, S, N, C, P, Si, or As.
 12. The organometallic compound of claim 1, wherein, in Formula 1, L₂ is a bidentate ligand represented by Formula 3:

wherein, in Formula 3, X₃₁ and X₃₂ are each O; X₃₁ is O and X₃₂ is N; or X₃₁ is N and X₃₂ is C,

indicates any atomic group linking X₃₁ and X₃₂ to each other, and * and *′ each indicate a binding site to M in Formula
 1. 13. The organometallic compound of claim 1, wherein, in Formula 1, L₂ is a group represented by one of Formulae 3A to 3F:

wherein, in Formulae 3A to 3F, Y₁₃ is O, N, N(Z₁), P(Z₁)(Z₂), or As(Z₁)(Z₂), Y₁₄ is O, N, N(Z₃), P(Z₃)(Z₄), or As(Z₃)(Z₄), T₁₁ is a single bond, a double bond, *—C(Z₁₁)(Z₁₂)—*′, *—C(Z₁₁)═C(Z₁₂)—*′, *═C(Z₁₁)—*′, *—C(Z₁₁)=*′, *═C(Z₁₁)—C(Z₁₂)═C(Z₁₃)—*′, *—C(Z₁₁)═C(Z₁₂)—C(Z₁₃)=*′, *—N(Z₁₁)—*′, or a C₅-C₃₀ carbocyclic group unsubstituted or substituted with at least one Z₁₁, a11 is an integer from 1 to 10, Y₁₁ and Y₁₂ are each independently C or N, T₂₁ is a single bond, a double bond, O, S, C(Z₁₁)(Z₁₂), Si(Z₁₁)(Z₁₂), or N(Z₁₁), ring CY₁₁ and ring CY₁₂ are each independently a C₅-C₃₀ carbocyclic group or a C₂-C₃₀ heterocyclic group, A₁ is P or As, Z₁ to Z₄ and Z₁₁ to Z₁₃ are each independently the same as defined in connection with R₂₁ in claim 1, d1 and d2 are each independently an integer from 0 to 10, and * and *′ each indicate a binding site to M in Formula
 1. 14. The organometallic compound of claim 1, wherein, in Formula 1, L₂ is a group represented by one of Formulae 3-1(1) to 3-1(66) and 3-1(301) to 3-1(309):

wherein, in Formulae 3-1(1) to 3-1(66) and 3-1(301) to 3-1(309), X₄₁ is O, S, N(Z₂₁), C(Z₂₁)(Z₂₂), or Si(Z₂₁)(Z₂₂), Z₁ to Z₄, Z_(1a), Z_(1b), Z_(1c), Z_(1d), Z_(2a), Z_(2b), Z_(2c), Z_(2d), Z₁₁ to Z₁₄, Z₂₁ and Z₂₂ are each independently the same as defined in connection with R₂₁ in claim 1, d14 is an integer from 0 to 4, d26 is an integer from 0 to 6, and * and *′ each indicate a binding site to M in Formula
 1. 15. The organometallic compound of claim 1, wherein the organometallic compound is one of Compounds 1 to 469:


16. An organic light-emitting device comprising: a first electrode; a second electrode; and an organic layer disposed between the first electrode and the second electrode and comprising an emission layer, wherein the organic layer comprises at least one organometallic compound of claim
 1. 17. The organic light-emitting device of claim 16, wherein the first electrode is an anode, the second electrode is a cathode, the organic layer further comprises a hole transport region between the first electrode and the emission layer and an electron transport region between the emission layer and the second electrode, the hole transport region comprises a hole injection layer, a hole transport layer, an electron blocking layer, a buffer layer, or any combination thereof, and the electron transport region comprises a hole blocking layer, an electron transport layer, an electron injection layer, or any combination thereof.
 18. The organic light-emitting device of claim 16, wherein the emission layer comprises the organometallic compound.
 19. The organic light-emitting device of claim 18, wherein the emission layer further comprises a host, and an amount of the host is larger than an amount of the organometallic compound.
 20. A diagnostic composition comprising the organometallic compound of claim
 1. 